Label: CERAVE AM FACIAL MOISTURIZING BROAD SPECTRUM SPF 50 SUNSCREEN- homosalate, octisalate, octocrylene and zinc oxide lotion
- NDC Code(s): 49967-263-01
- Packager: L'Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated June 28, 2024
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
-
Directions
For sunscreen use:
- apply liberally 15 minutes before sun exposure
- reapply at least every 2 hours
- use a water resistant sunscreen if swimming or sweating
- Sun Protection Measures. Spending time in the sun increases our risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
- limit time in the sun, especially from 10 a.m. - 2 p.m.
- wear long-sleeved shirts, pants, hats, and sunglasses
- children under 6 months of age: Ask a doctor
- Other information
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Inactive ingredients
water, glycerin, dimethicone, propanediol, butyloctyl salicylate, steareth-20, cellulose, niacinamide, ehtylhexyl methoxycrylene, steareth-2, ceramide NP, ceramide AP, ceramide EOP, sorbitan isostearate, carbomer, glycine soja (soybean) oil, triethoxycaprylsilane, cetearyl alcohol, behentriminium methosulfate, triethyl citrate, sodium hyaluronate, sodium lauroryl lactylate, cholesterol, ammonium polyacryloyldimethyl taurate, tocopherol, chlorphenesin, hydroxyacetophenone, caprylyl glycol, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer, trisodium ethylenediamine disuccinate, phytosphingosine, xanthan gum, polyhydrostearic acid, polysorbate 60, oryza sativa (rice) bran wax, benzoic acid, c12-22 alkyl acrylate/hydroxyethylacrylate copolymer
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INGREDIENTS AND APPEARANCE
CERAVE AM FACIAL MOISTURIZING BROAD SPECTRUM SPF 50 SUNSCREEN
homosalate, octisalate, octocrylene and zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-263 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 80 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 50 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 70 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) DIMETHICONE (UNII: 92RU3N3Y1O) PROPANEDIOL (UNII: 5965N8W85T) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) STEARETH-20 (UNII: L0Q8IK9E08) POWDERED CELLULOSE (UNII: SMD1X3XO9M) NIACINAMIDE (UNII: 25X51I8RD4) ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8) STEARETH-2 (UNII: V56DFE46J5) CERAMIDE NP (UNII: 4370DF050B) CERAMIDE AP (UNII: F1X8L2B00J) CERAMIDE 1 (UNII: 5THT33P7X7) SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) SOYBEAN OIL (UNII: 241ATL177A) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61) TRIETHYL CITRATE (UNII: 8Z96QXD6UM) HYALURONATE SODIUM (UNII: YSE9PPT4TH) SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO) CHOLESTEROL (UNII: 97C5T2UQ7J) AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (UNII: F01RIY4371) TOCOPHEROL (UNII: R0ZB2556P8) CHLORPHENESIN (UNII: I670DAL4SZ) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) CAPRYLYL GLYCOL (UNII: 00YIU5438U) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4) TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q) PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q) XANTHAN GUM (UNII: TTV12P4NEE) POLYHYDROXYSTEARIC ACID STEARATE (UNII: 8KQ7I65XZE) POLYSORBATE 60 (UNII: CAL22UVI4M) RICE BRAN (UNII: R60QEP13IC) BENZOIC ACID (UNII: 8SKN0B0MIM) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-263-01 1 in 1 CARTON 07/01/2024 1 89 mL in 1 PACKAGE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 07/01/2024 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'OREAL USA PRODUCTS, INC 624244349 manufacture(49967-263)