MENTHYL ANTHRANILATE
Official label name (INCIInternational name of cosmetic ingredients: the one printed on the pack. name, EU glossary of cosmetic ingredient names), No 16247
- No specific rule in the Cosmetics Regulation
MENTHYL ANTHRANILATE: no specific rule of the EU Cosmetics Regulation names it. It is neither prohibited nor restricted there, and it is on none of its lists of colorants, preservatives or UV filters. Annexes of the Regulation consulted on 23 October 2026.
Who it concerns
What official classifications and rules say for each group. A classification describes the hazard of the pure substance, not the risk of a product that contains it, which depends on the dose and the exposure.
Prohibition or serious classificationThe text prohibits the substance for this use, or ranks it among the most serious hazards (known or presumed carcinogenic, mutagenic or reprotoxic, identified endocrine disruptor).Worth watchingThe text sets a condition or flags a hazard worth knowing: allergen, suspected effect, condition for children, hazard to the aquatic environment.For informationOfficial information with no condition on a finished product: warning to read, irritation of the pure substance.
Pregnancy and breastfeeding
No classification harmonised by the European Union covers reproduction, the unborn child or breastfeeding for this substance. This does not mean it has been judged to have no effect during pregnancy.
Babies and children
The Cosmetics Regulation sets no age-related condition for this ingredient.
Skin, eyes and allergies
No harmonised classification for sensitisation, irritation or eye damage, and no obligation to label it as an allergen.
Environment
No harmonised classification as hazardous to the aquatic environment, and it is not on ECHAEuropean Chemicals Agency.'s Candidate List as an endocrine disruptor for the environment.
Read on the label
The Cosmetics Regulation requires no warning to be printed for this ingredient.
In plain words
What it is used for
Functions declared by manufacturers:
UV absorber: protects the cosmetic product from the effects of UV light.
Functions declared in the CosIngThe European Commission's database of cosmetic ingredients. inventory. CosIng, inventory of cosmetic ingredients (INCI names, CAS, EC, functions), retrieved 21 October 2026.
Definitions of functions (decision repealed on 8 May 2020, cited for information). Decision 2006/257/EC, inventory of cosmetic ingredients (definitions of functions), retrieved 22 October 2026.
What the rules say
No EU rule targets this ingredient specifically. It remains subject to the general rule: every product must undergo a safety assessment before it is sold (Article 10 of Regulation (EC) No 1223/2009), under the manufacturer's responsibility.
The text of the annexes
No specific rule of the EU Cosmetics Regulation names this ingredient: it is on none of its lists (prohibited, restricted, colorants, preservatives, UV filters). It may be used under the responsibility of the manufacturer, who must ensure the product is safe.
Search in Annexes II to VI. CosIng, Annex II of Regulation (EC) No 1223/2009 (prohibited substances), retrieved 23 October 2026, source updated 13 October 2026.
Identity
- CosIng identifier
- 78158
- CAS (according to CosIng)
- 134-09-8
- EC (according to CosIng)
- 205-129-8
- Declared functions
- UV absorber
CosIng inventory. CosIng, inventory of cosmetic ingredients (INCI names, CAS, EC, functions), retrieved 21 October 2026.
Elsewhere in the world
Information on other jurisdictions, with no effect on sale in France. What is covered, and what is not yet.
Comparison between countries
Most restrictive status in each country, and the maximum concentration cited. The details and the source of each rule follow.
| Country | Rule | Maximum concentration cited |
|---|---|---|
| European Union | No specific rule in the Cosmetics Regulation | not cited |
| United Kingdom | No specific rule in the Cosmetics Regulation | not cited |
| Switzerland | EU Regulation applies | not cited |
| United States (federal) | No federal rule recorded | not cited |
| Japan | No entry in the lists recorded | not cited |
| South Korea | Restricted differs from the EU | 5% |
| China | Not on the prohibited lists recorded (lists of allowed substances are not recorded) | not cited |
| Australia | Active ingredient allowed in sunscreens differs from the EU | 5% |
| Brazil | Allowed under conditions differs from the EU | 5% |
United Kingdom (Great Britain)
- No specific rule in the Cosmetics Regulation
Annexes II to VI in force. United Kingdom, Annexes II to VI of Regulation (EC) No 1223/2009 as retained and amended, retrieved 21 October 2026.
Contains public sector information licensed under the Open Government Licence v3.0.
Northern Ireland applies EU law.
Switzerland
Regulation (EC) No 1223/2009 applies in Switzerland (Article 54 of the Ordinance on Foodstuffs and Utility Articles).
Switzerland, FDHA Ordinance on Cosmetic Products (OCos, SR 817.023.31), consolidated version, retrieved 22 October 2026.
United States, federal rules
None of the integrated sections of the federal code (21 CFR 700.11 to 700.27 and 250.250) targets this name. The FDA does not publish a list of allowed ingredients.
United States, 21 CFR part 700 and section 250.250 (FDA rules on cosmetic ingredients), eCFR, retrieved 21 October 2026.
The eCFR is not an official legal edition of the Code of Federal Regulations.
South Korea
- Restricted: 멘틸안트라닐레이트 (MENTHYL ANTHRANILATE)
별표 2, 자외선 차단성분 (UV filters), entry 10, page 15. Limit: 5%.
South Korea, MFDS Regulation on Safety Standards for Cosmetics, Notification 2026-19, retrieved 22 October 2026.
Source: 식품의약품안전처 (MFDS), 화장품 안전기준 등에 관한 규정, via law.go.kr; table formatted by the publisher of this site.
Australia
- Active ingredient allowed in sunscreens: MENTHYL ANTHRANILATE
Permissible Ingredients Determination (No. 3) 2026, sunscreen actives, entry 3276, page 73. Thresholds cited: must not be more than 5%.
Conditions, source text
Purpose: A | Only for use in topical medicines for dermal application and not to be included in medicines intended for use in the eye. | The concentration in the medicine must not be more than 5%. | When used in primary sunscreen products, the following warning statements are required on the label: | - (AVOID) 'Avoid prolonged exposure in the sun' (or words to this effect); and | - (SUNPRO) 'Wear protective clothing - hats and eyewear when exposed to the sun' (or words to this effect).
Australia, Therapeutic Goods (Permissible Ingredients) Determination (No. 3) 2026, sunscreen actives, retrieved 22 October 2026.
Based on content from the Federal Register of Legislation at 2026-10-22. For the latest information on Australian Government legislation please go to https://www.legislation.gov.au. Licence CC BY 4.0.
Brazil
- Allowed under conditions: Antranilato de mentila MENTHYL ANTHRANILATE (MENTHYL ANTHRANILATE)
RDC 600/2022, Anexo (allowed UV filters), entry 8, page 2. Limit: 5%.
Brazil, ANVISA resolutions RDC 529/2021, 528/2021, 600/2022 and 628/2022, retrieved 22 October 2026.
Source: ANVISA. Text of the adopted draft resolutions, as the Official Journal could not be accessed; the 2021 lists of prohibited substances and preservatives were compared with the copy of the published text distributed by the State of Paraná, the 2022 lists of UV filters and colorants were not.
Recorded cosmetics that contain it
1 recorded product list it, according to Open Beauty Facts contributors. Records are dated: the formula may have changed. See the list (in French).
Open Beauty Facts, export of cosmetic products, retrieved 23 October 2026.
Data “Open Beauty Facts and its contributors”, licensed under ODbL 1.0 (opendatacommons.org/licenses/odbl/1-0); derived table distributed under the same licence.
Glossary: Commission Implementing Decision (EU) 2025/1175. Page updated on 23 October 2026.