quercetagetin est-il sûr pendant la grossesse ?
No EU cosmetic regulatory restriction or ban (Annex II/III) or harmonised CLP (ECHA Annex VI) classification was found for quercetagetin (CAS 90-18-6), and a search of available safety-assessment repositories (CIR/SCCS) returned no specific cosmetic safety opinion for this exact substance. PubChem lists the compound (CID 5281680) but there are no clear animal developmental/reproductive toxicity studies for topical exposure to quercetagetin in the peer‑reviewed literature—therefore default hazard (h=0), mechanism (m=0) and exposure (e=0) scores apply for pregnancy. (See PubChem entry and EU cosmetics/COSING and ECHA pages showing no specific restrictions or harmonised classification.)
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Frequently asked questions
- quercetagetin est-il sûr pendant la grossesse ?
- No EU cosmetic regulatory restriction or ban (Annex II/III) or harmonised CLP (ECHA Annex VI) classification was found for quercetagetin (CAS 90-18-6), and a search of available safety-assessment repositories (CIR/SCCS) returned no specific cosmetic safety opinion for this exact substance. PubChem lists the compound (CID 5281680) but there are no clear animal developmental/reproductive toxicity studies for topical exposure to quercetagetin in the peer‑reviewed literature—therefore default hazard (h=0), mechanism (m=0) and exposure (e=0) scores apply for pregnancy. (See PubChem entry and EU cosmetics/COSING and ECHA pages showing no specific restrictions or harmonised classification.)
- quercetagetin est-il sûr pendant l'allaitement ?
- No data specific to lactation or transfer into breast milk for quercetagetin was identified in regulatory or peer‑reviewed sources; no harmonised CLP or EU cosmetic restriction applies. In the absence of substance‑specific reproductive/lactation data, and given the lack of evidence of systemic reproductive hazard for this specific flavonoid, default scores are used (h=0, m=0, e=0).
- quercetagetin est-il sûr pour la peau de bébé ?
- No baby/infant (0–3 yr) topical safety data were identified for quercetagetin and no regulatory infant-specific restriction exists. Per the scoring rules, because there is measurable/possible dermal absorption for many small polyphenolic flavonoids (and no specific evidence showing zero absorption), exposure for baby skin is increased by +1 versus adult (adult e=0 → baby e=1) while hazard and mechanism remain default (h=0, m=0) absent infant-specific adverse data or harmonised classification.
- Comment VeriMom évalue-t-il quercetagetin ?
- VeriMom évalue quercetagetin à 100/100 (pas de risques connus) sur la base du statut EU CosIng, des classifications ECHA et des études PubMed.
- Quelles sont les alternatives sûres à quercetagetin pendant la grossesse ?
- Consultez notre liste d'alternatives sûres à quercetagetin basée sur une fonction similaire et une classification sans risques connus.
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Avis Médical
Ces informations sont fournies à titre éducatif uniquement et ne constituent pas un avis médical. Les scores de sécurité sont basés sur des données accessibles au public et peuvent ne pas refléter tous les risques. Consultez toujours votre professionnel de santé avant d'utiliser tout produit pendant la grossesse ou l'allaitement.