Compoatlas

STRONTIUM ACETATE

Official label name (INCIInternational name of cosmetic ingredients: the one printed on the pack. name, EU glossary of cosmetic ingredient names), No 27962

STRONTIUM ACETATE: Allowed with restrictions, with limits depending on the product type (Annex III, entry 58), under Regulation (EC) No 1223/2009. Annexes of the Regulation consulted on 21 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

    Worth watchingThe text sets a condition or flags a hazard worth knowing: allergen, suspected effect, condition for children, hazard to the aquatic environment.

    Worth watchingThe text sets a condition or flags a hazard worth knowing: allergen, suspected effect, condition for children, hazard to the aquatic environment. Annex III, entry 58, sets a condition for children: “Frequent use by children is not advisable”

    For a question about your own situation, ask your doctor, midwife or pharmacist.

  • Skin, eyes and allergies

    No official classification for sensitisation, irritation or eye damage, and no obligation to label it as an allergen.

  • Environment

    No official classification as hazardous to the aquatic environment and no assessment as an endocrine disruptor for the environment.

  • Read on the label

    For informationOfficial information with no condition on a finished product: warning to read, irritation of the pure substance.

    For informationOfficial information with no condition on a finished product: warning to read, irritation of the pure substance. Annex III, entry 58, requires this to be printed on the pack: “Contains strontium acetate Frequent use by children is not advisable”.

In plain words

What it is used for

Functions declared by manufacturers:

Oral care: provides cosmetic effects to the oral cavity, e.g. cleansing, deodorising, protecting.

Soothing: helps lightening discomfort of the skin or of the scalp.

What the rules say

Allowed, with restrictions: Annex III sets a maximum concentration, the product types allowed and a warning to be printed on the packaging. Ingredient lists do not give quantities, so the concentration cannot be checked on the label; the warning can.

The text of the annexes

Allowed with restrictions

Product type
Oral products
Maximum concentration
3.5% (as strontium) When mixed with other permitted strontium products the total strontium content must not exceed 3.5%
Warning to print
Contains strontium acetate Frequent use by children is not advisable
Entry
Annex III, No 58
Substance
Strontium acetate hemihydrate
Glossary names
STRONTIUM ACETATE
CAS
543-94-2
EC
208-854-8

What has changed, and what will change

Dates of the texts that cover this ingredient. A text date may cover several substances: the details of each entry are below.

  1. Annex III, entry 58: introduced or replaced by Regulation (EC) No 1223/2009

  2. Annex III, entry 58: applies from this date

Identity

CosIng identifier
38353
CAS (according to CosIng)
543-94-2
EC (according to CosIng)
208-854-8
Declared functions
Oral care, Soothing
Wikidata
Q1674310
ECHAEuropean Chemicals Agency. InfoCard
100.008.050
InChIKey
RXSHXLOMRZJCLB-UHFFFAOYSA-L

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.

CountryRuleMaximum concentration cited
European UnionAllowed with restrictions3.5%
United KingdomAllowed with restrictions3.5%
SwitzerlandEU Regulation applies3.5%
United States (federal)No federal rule recordednot cited
JapanNo entry in the lists recordednot cited
South KoreaNo entry in the lists recordednot cited
ChinaNo entry in the lists recordednot cited
AustraliaNo entry in the lists recordednot cited
BrazilNo entry in the lists recordednot cited

United Kingdom (Great Britain)

  • Allowed with restrictions (Annex III)

Same entries as in the European Union. Conditions (concentrations, warnings) may differ: they are not compared here.

Switzerland

Regulation (EC) No 1223/2009 applies in Switzerland (Article 54 of the Ordinance on Foodstuffs and Utility Articles).

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.

Recorded cosmetics that contain it

2 recorded products list it, according to Open Beauty Facts contributors. Records are dated: the formula may have changed. See the list (in French).

Glossary: Commission Implementing Decision (EU) 2025/1175. Page updated on 21 October 2026.