CERAVE FACIAL MOISTURIZING WITH SUNSCREEN BROAD SPECTRUM SPF 30 FOR NORMAL TO DRY SKIN- homosalate, octinoxate, octisalate, octocrylene and zinc oxide lotion
Drug Labeling and Warnings
Drug Details [pdf]
- Active ingredients (w/w) / Ingrédients actifs (p/p)
- Directions / Mode d'emploi
- Warnings / Mises en garde
- Do not use / Ne pas utiliser
- When using this product / Lorsque vous utilisez ce produit
- Stop use and ask a doctor if / Cesser d'utiliser et consulter un médecin si
- Keep out of reach of children. / Garder hors de la portée des enfants.
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Inactive ingredients / Ingrédients inactifs
Aqua, Niacinamide, Cetearyl alcohol, Glycerin, Propanediol, Dimethicone, Behentrimonium methosulfate, Phenoxyethanol, Aluminum starch octenylsuccinate, Hydroxyethylcellulose, Hydroxyacetophenone, Triethoxycaprylylsilane, Trisodium ethylenediamine, disuccinate, Sodium lauroyl lactylate, Sodium hyaluronate, Ceramide NP, Triethyl citrate, BHT, Caprylyl glycol, Ceramide AP, Phytosphingosine, Cholesterol, Carbomer, Xanthan gum, Benzoic acid, Disodium phosphate, Polysorbate 60, Sodium phosphate, Ceramide EOP.
- Questions?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CERAVE FACIAL MOISTURIZING WITH SUNSCREEN BROAD SPECTRUM SPF 30 FOR NORMAL TO DRY SKIN
homosalate, octinoxate, octisalate, octocrylene and zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 82046-400 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 100 mg in 1 mL OCTINOXATE (UNII: 4Y5P7MUD51) (ETHYLHEXYL METHOXYCINNAMATE - UNII:4Y5P7MUD51) OCTINOXATE 50 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (ETHYLHEXYL SALICYLATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 20 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 80 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) NIACINAMIDE (UNII: 25X51I8RD4) CETEARYL ALCOHOL (UNII: 2DMT128M1S) GLYCERIN (UNII: PDC6A3C0OX) PROPANEDIOL (UNII: 5965N8W85T) DIMETHICONE (UNII: 92RU3N3Y1O) BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61) PHENOXYETHANOL (UNII: HIE492ZZ3T) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) HYDROXYETHYLCELLULOSE (UNII: T4V6TWG28D) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q) SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO) SODIUM HYALURONATE (UNII: YSE9PPT4TH) CERAMIDE NP (UNII: 4370DF050B) TRIETHYL CITRATE (UNII: 8Z96QXD6UM) BHT (UNII: 1P9D0Z171K) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CERAMIDE AP (UNII: F1X8L2B00J) PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q) CHOLESTEROL (UNII: 97C5T2UQ7J) CARBOMER (UNII: 0A5MM307FC) XANTHAN GUM (UNII: TTV12P4NEE) BENZOIC ACID (UNII: 8SKN0B0MIM) DISODIUM PHOSPHATE (UNII: 22ADO53M6F) POLYSORBATE 60 (UNII: CAL22UVI4M) SODIUM PHOSPHATE (UNII: SE337SVY37) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 82046-400-01 1 in 1 CARTON 05/13/2028 1 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC: 82046-400-02 1 in 1 CARTON 05/13/2028 2 89 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date export only 05/13/2026 Labeler - L’Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'OREAL USA PRODUCTS, INC. 624244349 manufacture(82046-400)
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