Label: NEUTROGENA CLEAR FACE SERUM FRAGRANCE FREE SPF 60 PLUS- avobenzone, homosalate, octisalate, octocrylene liquid
- NDC Code(s): 69968-0777-2
- Packager: Kenvue Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 12, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Uses
- Warnings
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Directions
▪ apply liberally 15 minutes before sun exposure
▪ reapply: ▪ after 80 minutes of swimming or sweating ▪ immediately after towel drying ▪ at least every 2 hours
▪ Sun Protection Measures. Spending time in the sun increases your 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, Butyloctyl Salicylate, Glycerin, Alcohol Denat., Silica, Dimethicone, Camellia Sinensis Leaf Extract, Aluminum Starch Octenylsuccinate, Polyurethane-62, Phenoxyethanol, Pentylene Glycol, Sodium Acryloyldimethyltaurate/VP Crosspolymer, Bisabolol, Acrylates/Dimethicone Copolymer, Glyceryl Stearate, Chlorphenesin, Styrene/Acrylates Copolymer, Menthyl Lactate, Tocopheryl Acetate, Disodium EDTA, Trideceth-6, Butylene Glycol, Sodium Hydroxide
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 50 mL Carton
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INGREDIENTS AND APPEARANCE
NEUTROGENA CLEAR FACE SERUM FRAGRANCE FREE SPF 60 PLUS
avobenzone, homosalate, octisalate, octocrylene liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0777 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 135 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 100 mg in 1 mL Inactive Ingredients Ingredient Name Strength 2-ETHYLHEXYL ACRYLATE, METHACRYLATE, METHYL METHACRYLATE, OR BUTYL METHACRYLATE/HYDROXYPROPYL DIMETHICONE COPOLYMER (30000-300000 MW) (UNII: S7ZA3CCJ4M) TRIDECETH-6 (UNII: 3T5PCR2H0C) GREEN TEA LEAF (UNII: W2ZU1RY8B0) PHENOXYETHANOL (UNII: HIE492ZZ3T) PENTYLENE GLYCOL (UNII: 50C1307PZG) BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) CHLORPHENESIN (UNII: I670DAL4SZ) MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) SODIUM HYDROXIDE (UNII: 55X04QC32I) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) GLYCERIN (UNII: PDC6A3C0OX) ALCOHOL (UNII: 3K9958V90M) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) DIMETHICONE (UNII: 92RU3N3Y1O) LEVOMENOL (UNII: 24WE03BX2T) POLYURETHANE-62 (UNII: TBK645J3J8) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0777-2 1 in 1 CARTON 10/19/2022 1 50 mL in 1 BOTTLE, PUMP; 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 10/19/2022 Labeler - Kenvue Brands LLC (118772437)