Label: COPPERTONE SPORT FACE SPF 60 PLUS SUNSCREEN- avobenzone 3%, homosalate 15%, octisalate 5%, octocrylene 10% lotion
- NDC Code(s): 66800-9013-4
- Packager: Beiersdorf Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 30, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients
- Purpose
- Use
- Warnings
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
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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-sleeve shirts, pants, hats, and sunglasses
■ children under 6 months: Ask a doctor
- Other information
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Inactive ingredients
water, styrene/acrylates copolymer, butyloctyl salicylate, diethylhexyl 2,6-naphthalate, polyester-7, cetearyl alcohol, glyceryl stearate, silica, neopentyl glycol diheptanoate, 1,2-hexanediol, copernicia cerifera (carnauba) wax, PPG-15 stearyl ether, silica dimethyl silylate, tapioca starch, tocopheryl acetate, sodium ascorbyl phosphate, sodium stearoyl glutamate, diethylhexyl syringylidenemalonate, tocopherol (vitamin E), hydroxyacetophenone, argania spinosa kernel oil, xanthan gum, glycereth-26, glycerin, disodium EDTA, bisabolol
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INGREDIENTS AND APPEARANCE
COPPERTONE SPORT FACE SPF 60 PLUS SUNSCREEN
avobenzone 3%, homosalate 15%, octisalate 5%, octocrylene 10% lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66800-9013 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 15 g in 100 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 g in 100 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g in 100 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 10 g in 100 g Inactive Ingredients Ingredient Name Strength DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM) PPG-15 STEARYL ETHER (UNII: 1II18XLS1L) WATER (UNII: 059QF0KO0R) STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) DISODIUM EDTA-COPPER (UNII: 6V475AX06U) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W) POLYESTER-7 (UNII: 0841698D2F) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) XANTHAN GUM (UNII: TTV12P4NEE) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) .ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC) TOCOPHEROL (UNII: R0ZB2556P8) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) STARCH, TAPIOCA (UNII: 24SC3U704I) SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024) DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248) CARNAUBA WAX (UNII: R12CBM0EIZ) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) ARGANIA SPINOSA WHOLE (UNII: 83K6O4FR76) SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR) GLYCERETH-26 (UNII: NNE56F2N14) Product Characteristics Color white (white to off-white) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66800-9013-4 74 g in 1 TUBE; Type 0: Not a Combination Product 11/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 11/01/2023 Labeler - Beiersdorf Inc (001177906)
