New R3337 Food Labelling Regulations: What Every South African Food Business Must Do Now

By Mthokozisi Nkosi, Food Safety & Regulatory Consultant, ASC Food Safety

South African food labels being assessed for draft R3337 readiness: nutrition compliance, claims and warning label exposure

If you manufacture, pack, import or retail food in South Africa, the single biggest regulatory shift of the decade is heading your way. Draft R3337, published for public comment in late 2023, is set to replace R146 of 2010 as the country’s food labelling law. To be clear from the outset: R3337 is still a draft as of mid-2026 and is not yet in force. R146 remains the law you must comply with today. But finalisation is expected, and the businesses that treat the draft as a planning document rather than a distant rumour will be the ones that keep their products on shelf without a last-minute scramble.

At ASC Food Safety, our regulatory work for leading pharmaceutical and FMCG brands, including names like Adcock Ingram, KFC Africa / Yum! Brands, Spur Corporation and Kellogg’s, has taught us one consistent lesson: labelling transitions are never as far away as they feel, and artwork pipelines are always slower than anyone budgets for. This article sets out where R3337 stands, what is changing, and a practical roadmap to get ahead of it.

Where R3337 Stands Right Now

South African food labels are currently governed by R146 of 2010: the Regulations Relating to the Labelling and Advertising of Foodstuffs, made under the Foodstuffs, Cosmetics and Disinfectants Act 54 of 1972. R146 has been the backbone of label compliance for over fifteen years, covering everything from ingredient lists and allergen declarations to date marking and prohibited claims.

Draft R3337 was published by the Department of Health for public comment in late 2023 and is intended to replace R146 entirely. The comment period generated significant industry response, and the Department has been working through submissions since. As of mid-2026, the regulation has not been finalised or gazetted into force, but finalisation is expected, and the direction of travel is unmistakable. When it lands, there will be a transition period, and every label in your portfolio will need to be reviewed against the new requirements.

The mistake we see repeatedly is businesses treating “still a draft” as “nothing to do yet”. The draft tells you, in considerable detail, what the Department of Health intends to require. Ignoring that signal is a commercial risk, not a saving.

R3337 vs R146: The Key Changes

1. Mandatory front-of-pack warning labels

The headline change. Draft R3337 introduces mandatory front-of-pack warning labels, modelled on Chile’s black warning system, for products high in sugar, sodium or saturated fat, and for products containing artificial sweeteners. If your product exceeds the thresholds, a prominent warning must appear on the front of the pack. For many South African brands, this is the first time the front of the pack (the marketing real estate) becomes regulated compliance territory. We unpack this fully in our companion article on front-of-pack warning label preparation.

2. Restrictions on marketing to children

Products carrying front-of-pack warnings face restrictions on marketing directed at children: think cartoon characters, toys, celebrity endorsements aimed at minors, and child-directed claims. For confectionery, snacks, cereals and beverages, this cuts to the heart of long-standing brand strategies.

3. Stricter allergen and gluten-free claim rules

R146 already requires declaration of common allergens: egg, cow’s milk, crustaceans and molluscs, fish, peanuts, soybeans, tree nuts, and gluten-containing cereals. Draft R3337 tightens the framework further, including stricter rules around gluten-free claims and how allergen information must be presented. If your allergen management programme is built on habit rather than validated controls, now is the time to fix it.

4. Tighter nutrition and health claims

The draft imposes a far more rigorous regime for nutrition and health claims. Claims that products high in sugar, sodium or saturated fat currently carry, such as “source of energy” and “with added vitamins”, face restriction where the product qualifies for a warning label. Substantiation requirements become sharper across the board. Every claim on every pack in your range will need to be re-justified, not just re-typeset.

5. A full-portfolio artwork impact

Beyond the headline items, R3337 revises requirements across the label: nutritional information presentation, ingredient declarations, and the interaction between claims and warnings. In practice, very few labels will pass unchanged. Multiply that across a 40-SKU portfolio, add design, translation, proofing, plate-making and packaging stock run-down, and you begin to see why early planning matters.

Key Takeaways

  • R146 of 2010 is still the law. Draft R3337 is not yet in force, but it is expected to be finalised and will replace R146.
  • The biggest changes: front-of-pack warning labels, marketing-to-children restrictions, stricter allergen and gluten-free rules, and tighter nutrition and health claims.
  • Almost every label in a typical portfolio will need review. Artwork pipelines take longer than transition periods feel.
  • Early movers protect shelf space, avoid packaging write-offs, and can reformulate on their own timeline instead of the regulator’s.
  • A gap assessment against the draft now is the cheapest insurance you can buy.

Your R3337 Preparation Roadmap

Here is the phased approach we run with clients, from single-product start-ups to JSE-listed manufacturers.

Phase 1: Portfolio gap assessment (do this now)

Audit every SKU against both R146 (current compliance: you would be surprised how many labels fail the existing law) and draft R3337. For each product, establish: Would it trigger a front-of-pack warning? Which claims would fall away? What allergen presentation changes apply? The output is a risk-ranked register of your entire range.

Phase 2: Reformulate or relabel decisions

For every product that would carry a warning, you face a strategic choice: reformulate below the thresholds, or accept the warning and adjust positioning. Reformulation takes months: recipe trials, shelf-life validation, sensory work, costing. That is precisely why this decision cannot wait for the final gazette. Products that reformulate early avoid the warning entirely; products that wait wear it while their competitors do not.

Phase 3: Claims and artwork pipeline

Rebuild your claims register with substantiation files, then sequence artwork changes by commercial priority and packaging stock levels. Coordinate with procurement so you are not writing off millions of rands in printed film and cartons when the transition deadline arrives.

Phase 4: Train your people

Your NPD, marketing, QA and procurement teams all touch labelling decisions. A marketing manager who understands why “high in energy” is a regulatory claim, not just copy, saves you redesign cycles. Our accredited training arm offers the Essentials of Food Labelling Claims for Food Manufacturing course online and self-paced, alongside 25+ other food safety courses.

Phase 5: Monitor finalisation and execute

When R3337 is gazetted, the businesses with a completed gap assessment and pre-approved artwork concepts simply press go. Everyone else joins the queue at design agencies, printers and consultants, all at once.

Why Acting Before Finalisation Wins Shelf Space

Retail buyers do not wait for gazettes. Major South African retailers are already asking suppliers about R3337 readiness, because a supplier who cannot transition on time is a supplier who leaves a gap on shelf. Demonstrating a documented readiness plan is becoming a listing advantage.

There is also the enforcement dimension. Non-compliant labels expose you to product recalls, Port Health detentions at the point of entry for imported goods, and National Consumer Commission action. None of these are hypothetical. They are the routine consequences of labels that fail inspection. And every one of them costs multiples of what proactive compliance costs.

Finally, there is the quiet competitive upside: a reformulated product that avoids a warning label, launched before the regulation bites, effectively gets a head start the market will not see coming until it is too late to copy.

Book a Label Compliance Review

Get every SKU assessed against R146 and draft R3337 by the team trusted by Adcock Ingram, KFC Africa, Spur and Kellogg’s, with a 48-hour label review option available.

Book a Consultation +27 41 004 0382 info@ascfoodsafety.com

For the full picture of how we support labelling and regulatory compliance end to end (label reviews, claims substantiation, import support and Port Health readiness), visit our Labelling & Regulatory Advisory service page.

Draft R3337 clause by clause

This section was previously published as a separate article. It is kept here so the strategic view and the clause by clause detail sit on one page. It sets out what each regulation in the draft would change, as at 8 September 2026, when R3337 remained a draft.

What are the Labelling and Advertising Regulations?

The Labelling and Advertising Regulation is a legal document that aims to ensure that South African consumers are appropriately informed of the food they consume and places the responsibility for providing information on food businesses. In addition, these regulations have been drafted to protect consumers from misinformation, misrepresentation, mislabelling and incomplete information. Most of what is contained in these regulations is what first-world countries have already implemented.

The labelling and advertising R146 was published by the Minister of Health on 1 March 2010 in terms of the Foodstuff, Cosmetics and Disinfectant Act 1972 (52 of 1972). The Regulation only came into effect on 1 March 2012 after granting a grace period of 2 years to the food industry to comply with the regulation requirements since the new requirements had logistical and operational impacts on the food industry.

Compliance with the requirements of these regulations is enforced by Environmental Health Practitioners (EHPs) employed by Municipal Health Services of Metro and District Municipalities.

Non-compliance leads to the EHP issuing the non-complying company with a notice of compliance, allowing them time to comply. Persistent non-compliance may lead to legal steps being taken and prosecution.

In 2014, the Department of Health proposed further significant amendments to the Regulation, published as Regulation R429 of 2014. The Regulation R429 of 2014 was never promulgated.

Early this year, the Department published several draft regulations for labelling, with the final draft being Labelling and Advertising of Foodstuff Regulation R3337, which, if finalised based on stakeholder feedback, will replace regulations R146 completely. The draft regulation has been open for public comments since 21 April 2023, and the opportunity to submit will be closed on Friday (21 July 2023).

DOWNLOAD A SUMMARY OF THE DIFFERENT VERSIONS OF LABELLING REGULATIONS HERE

Labelling and Advertising Regulations Timeline:

  • Before 1993: Basic Regulations under the FCD Act
  • 1993-2010: Regulation 2043 (Came into effect in 1995)
  • 2010: R 146 (Most comprehensive covering gaps)
  • 2014: Version 2 of R146, which is Regulation R429 (Covered more gaps but was never promulgate.

With the new Regulation in the pipeline, what can you, as the Food Handler (including consumers, manufacturers, packers, retailers, street vendors and NGOs) expect from this new Regulation when it comes into effect?

This Article will discuss some of the changes with the new draft regulation R3337. We will not discuss the contents of the current Labeling and Advertising regulations R146..

Overview of the Draft Regulations R3337

The current draft in question has a total of 249 pages compared to regulation R146 which has a total of 51 pages, and the then-proposed amendment R429, with has a total of 106 pages. The number of regulatory requirements will be significant with the latest update.

The draft regulation (R3337) also has a total of 78 sections. The current Regulation has 56 sections/ The new draft, therefore, has 22 more sections compared to the current Regulation R146.

There are, finally, many changes in terms of definitions.

A total of 47 definitions have been removed, and about 32 new terms have been proposed. We will look at two or three critical additions to note.

The draft regulation (R3337) is more reader-friendly by including tables under each section and referencing them accordingly under each section of the Regulation.

The draft regulation has four more new annexures.

  • Annexure 6: Major dietary carbohydrates
  • Annexure 7: Culinary Herbs and Spices for ordinary use in food preparations
  • Annexure 8: South African Nutrient Profiling Model: Screening Criteria for Health and nutrition claims
  • Annexure 9: Illustrative list of foods that need only a “date of manufacture” or a “date of packaging”, as appropriate
  • Annexure 10: Front of Pack Nutrition Labelling (FOPL) logos

The draft regulation has stopped referring to the SANS. Instead, it has referenced the relevant Acts, also included in the definitions.

Important Key Changes

  • Permitted and Prohibited Claims
  • Prohibited trademarks and trade names.
  • Marketing restrictions on unhealthy foods
  • Front of the pack health warning
  • Artificial Sweeteners and Sugar
  • Interpretation Issues (Guidelines) still need to be published.

New Definitions on Draft R3337

We will not be discussing all new definitions in-depth, but we have picked up a few which are very important to note:

Best Quality Before Date: exact definition as Best Before Date with a new addition:
‘…However, beyond the date, the food may still be acceptable for consumption.’
The long-standing debate around the best-before date has been addressed in the new Regulation. The definition of best before has been changed to accommodate the fact that food might still be acceptable for consumption after the best before as much as food can spoil before the best before date.

New Definitions on Draft R3337
We will not be discussing all new definitions in-depth, but we have picked up a few which are very important to note:

  1. Best Quality Before Date: exact definition as Best Before Date with a new addition: ‘…However, beyond the date, the food may still be acceptable for consumption.’ The long-standing debate around the best-before date has been addressed in the new Regulation. The definition of best before has been changed to accommodate the fact that food might still be acceptable for consumption after the best before as much as food can spoil before the best before date.
  2. The additive definition has excluded processing aid, and regulation 36 has included additional requirements for processing aid not to be declared.
  3. Children’s definition for Front Of Package Labeling (FOPL) marketing included all children 18 years and under.

Specific Changes Under Each Regulation

Below we will discuss some changes you will notice in the draft regulation. One of the noticeable changes that you will see throughout the Regulation is that ‘shall’ has been replaced with ‘must’ in the draft regulation. This has been done to reinforce the mandatory aspect of the requirements.
Let’s further discuss some of the changes you will see in the specific section of the draft regulation:

Regulation 2, General

Sub-regulation 2 has been slightly updated in wording, but the requirement has remained unchanged.

Subregulation 3 has been made more explicit regarding who is responsible for the complaint of product labels with these requirements. The person whose business or business name is marketing the foodstuff for sale is responsible.

Sub-regulation 4 further outlines on the new draft (Subject to regulation 74 (3)) that any information required by the Regulation but not included on the product’s label must be provided immediately upon request. Meaning it must be kept in the store where the products are sold.

The rest of the requirements are similar to those in R146. However, the presentation of the requirements or the wording and order is different. The requirements, however, have stayed the same.

Regulation 3 – Presentation

The requirements under Regulation 3 have stayed the same. A few additions have been made:

3(1) Subject to regulation 4, the information that must appear on any label must be – in English, and where label space permits, a second official language of South Africa of the manufacturer’s choice: Provided that the minimum letter size used for the required label information may not be reduced to accommodate various languages for local or export purposes
.
NB: This is meant to clarify that the second optional language can be added on the label provided it does not affect the visibility of the primary labelling language, English.

Section 1(b) has another edition on the contract of the label stating that it should be indelible, clearly visible, and easily legible with a significant contrast between font colour and background colour, and the legibility thereof must not be affected by pictorial or any other matter, printed or otherwise.; Provided that –

(i) colours used on labels shall not dominate/ overwhelm nor be used in such a way that any information, warning statement or FOPL logos, when applicable, become poorly visible, non-legible or indistinguishable from pictorial representations and information; and

(ii) White lettering on any background colour except black shall be prohibited.

N.B The draft regulation has highlighted the need to refrain from using creativity that might hinder consumers from accessing important information about the product.

Regulation 6 – Country of Origin

There is a significant change under Regulation 6. The amendment regulation prohibited the use of national flags. The new draft regulation permits using national flags when referring to the country of origin.

2(a) Using a national flag is only permitted to indicate the country of origin when accompanied by the wording contemplated in sub-regulation (1).

2(b) In the case where the wording” Proudly South African” is used, the South African Flag may be used, provided the product complies with the criteria for “Products of (name of country).

Regulation 8- Date Mark

Numerous changes are made under this Regulation; we will only highlight a few important ones, like the sale of foodstuff that has passed their Best Before Quality Date is permitted, provided the integrity of the food has been maintained. This has two exceptions:

  1. Enhanced food stuff sold to children
  2. Imported Foodstuff.

The importance of including the date of manufacture has also been highlighted under the draft regulation.

  • Best Before Quality Date has been added under section 2
  • The expiration date has been included under section 6(a)

Regulation 9- Prohibited

Under regulation 9 (a), the following additions are noted All endorsed foodstuff ( By credible endorsing bodies) must comply with the following foodstuff, which is endorsed, successfully qualifies with the screening criteria of the Nutrient Profiling Model for South Africa as outlined in Annexure 8 using the electronic calculator which is available on the website of the Department and is not required to bear any Front-of-pack-logo (FOPL); and

There is also a change in the fibre content and sugar percentage in endorsed fruit or vegetable juice. Below is the new requirement:

In the case of fruit or vegetable juices being endorsed, the fruit or vegetable juice does not contain any added sugars or free sugars, qualifies for the non-addition claim for sugars and has an intrinsic dietary fibre content per 100 ml that equals at least 20% of the dietary fibre content of 100 g of the same fresh fruit or vegetable; provided the dietary fibre is the intrinsic natural fibre from fruit or vegetable pulp/purees/pastes and not added purified non-starch polysaccharides (NSP);

There have been new requirements included in terms of wine and alcohol. Subsection four covers all these requirements.

Regulation 24, Bulk Stock

There is a significant additional requirement on the bulk stork under sub-regulation 3. It outlines requirements for foodstuffs that are packed in bulk, and there is additional packaging that covers labels. There is a significant addition in the labelling information that must be provided on the bulk packaging above the additional packaging:

(a) Name of the product; (b) name and address of the manufacturer; (c) special storage conditions; (d) allergen information; (e) batch code; (f) an appropriate date marking.

There is also an additional requirement for bulk storage of cheese and deli-type processed meat loaves; they must have a packaging date and repackaging date when sliced and reparked.

Regulation 25, Small Packages

Regulation 25 states that the packaging of a pre-packaged foodstuff that has a total exterior area of 2000mm﮹² or less, including single once-off use 10g or less sized packages of culinary herbs and spices, sauces, and condiments and 25g or less sized confectionary products are exempted from the requirements of labelling.

The new draft regulation has one new addition, including the FOPL logo, where applicable.

Regulation 27, Vending Machines

Vending Machines products have one crucial additional requirement on the visibility of the FOPL.
Pre-packaged foodstuffs which are required to bear a mandatory Front-of-pack label (FOPL) shall be packed in the vending machine in such a way that clearly displays the foodstuff with the main panel on which the FOPL logos are clearly visible from the outside of the machine.

This will ensure that the consumers see the warning labels before they purchase the product.

Regulation 29, Prepacked Food Additive

The requirement now states that the labelling of prepacked food additives must comply with the requirements of the latest edition of the Codex general standard for labelling food additives.

The requirement states that pre-parked additives do not have to include a nutritional table.

Regulation 30, Flavourants

There is one additional requirement under this section for compound flavourant labelling:

4) Subject to regulation 20, mixtures containing one or more flavourings, other ingredients such as salt, sugar, herbs, spices or other categories of food additives intended for use in or on snack foods or in other foodstuffs must be considered as being compound ingredients and must be labelled accordingly.

Regulation 31, Artificial Sweeteners (Additives)

This is a new requirement in draft R3337, which outlines labelling requirements for foodstuffs with artificial sweeteners.

Regulation 32 – Modified Starches, Processing Aids and Carry-over of Additives

Additional requirements are as follows:

  • Declaration of processing method of modified starches
  • Requirement not to declare preparation utensils.
  • Declaration of additives and preservatives used.

Regulation 37, Allergens

This section on the draft regulation has grown significantly several additional requirements have been included.

  • The requirement to declare sulphates when their amount is equal to or less than 10 ppm.
  • A list of products derived from allergens is under subsection 2, exempted from the allergen labelling requirement.

Regulation 38, Uncommon Allergens

There is an additional requirement for declaring products made of/or containing a part of Lupin. The following labelling is required: “Allergenicity: Peanut-allergic individuals are at high risk to react to lupin present in this product.”

Regulation 42, Nutritional Information/Facts

There are numerous changes and additions that you will find under this section of the drafts regulation:

The exemption for having a nutritional table does not only include the vendors or home industry on the draft regulation but also includes products listed under table one. The exemption only applies if no health claim is made on the product.

There are also more detailed requirements on the values and structure of the nutritional table, including the credibility of the information provided.

Regulations 47, Additional Requirements Relating to the Nutritional Information Table

There are several essential requirements under this section, mainly concerning laboratory tests; specifications of nutritional laboratory test methodologies.

Regulation 50, Nutrient Profiling Made for Nutrient and Food Claim

Food businesses will need to consider several crucial additions under this Regulation. One of them is products that exceed requirements on key nutrients or have artificial sweeteners that must have FOPL (Front Of Pack Label) on the main panel to warn consumers.

Regulation 51, Profiling Model For Foodstuffs For South Africa For The Purpose Of FOPL Logo On Labels Of Foodstuff That May Not Be Marketed Or Advertised To Children

Firstly, prepacked foodstuff must bear a Font of Park Label Logo if it contains saturated fat, sugar and sodium. Secondly, if it exceeds the nutrient cut-off limit of Total sugar, total sodium and total saturated fatty acids as per requirements under this section and finally, if it contains artificial sweeteners.

Requirements for FOPL are described under Annexure 10 of the draft regulation. The logo is required to cover about 25% of the front pack. More requirements prohibit the use of different tactics to encourage consumers to buy items with FOPL, which are listed under the requirements of the Regulation, like competitions, using celebrities and portraying happy families, and so much more.

Finally, products with FOPL must show the below warning label during advertisements.

WARNING: This product is high in [insert key nutrients] / contains artificial sweeteners. Excessive consumption may be detrimental to your health.

Completely New Additions

  • Regulation 53: Use of South African Food-Based Dietary Guidelines
  • Regulation 54: Claims on packaged water
  • Regulation 55: Foodstuffs containing added purified, crystalline fructose (C6H12O6) or added non-nutritive sweeteners.
  • Regulation 56: Fake foodstuffs
  • Regulation 57: Cosmetic claims
  • Regulation 58: Claims represented through pictures

The rest of the Regulation guides nutritional and health claims, respectively. The draft outlines specific requirements for prohibited and allowed claims depending on the product you are handling.

DOWNLOAD A SUMMARY OF THE DIFFERENT VERSIONS OF LABELLING REGULATIONS HERE

Frequently Asked Questions

Is R3337 already law in South Africa?

No. R3337 is a draft regulation published for public comment in late 2023. As of mid-2026 it has not been finalised, and R146 of 2010 remains the current food labelling law. Finalisation is expected, however, so preparation should already be underway.

What is the biggest change in draft R3337 compared to R146?

Mandatory front-of-pack warning labels for products high in sugar, sodium or saturated fat, modelled on Chile’s system, together with restrictions on marketing those products to children, stricter allergen and gluten-free claim rules, and tighter nutrition and health claims.

How long will businesses have to comply once R3337 is finalised?

The final regulation is expected to include a transition period, but its length is not yet confirmed. Experience with previous labelling transitions shows that artwork, reformulation and packaging stock run-down consume transition periods faster than expected, which is why gap assessments should happen before finalisation.

Does R3337 affect imported foods?

Yes. Imported foods sold in South Africa must comply with South African labelling law, and non-compliant consignments risk Port Health detention at the point of entry. Importers should assess their ranges against both R146 and the draft now.

What should my business do first?

Commission a portfolio gap assessment against R146 and draft R3337. It identifies which products would trigger warnings, which claims are at risk, and where reformulation makes commercial sense, giving you a risk-ranked action plan before the final regulation lands.

ASC Food Safety Consultants. Leading with Science. Ensuring Food Safety. Serving clients from Gqeberha, Johannesburg, Cape Town and Durban, with nationwide virtual support. Rated 4.9/5 from 1,200+ Google reviews.

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