Label: COPPERTONE OIL FREE AND SHINE CONTROL FACE SUNSCREEN SPF 45- avobenzone 3%, homosalate 10%, octisalate 5%, octocrylene 10% lotion
- NDC Code(s): 66800-8164-2
- Packager: Beiersdorf Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 27, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients
- Purpose
- Use
- Warnings
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
-
Directions
■ apply liberally 15 minutes before sun exposure
■ reapply:
■ after 40 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
-
Inactive ingredients
water, alcohol denat., butyloctyl salicylate, silica,bis-octyldodecyl dimer dilinoleate/propanediol copolymer, glyceryl stearate, tapioca starch, behenyl alcohol, butylene glycol dicaprylate/dicaprate, C12-15 alkyl benzoate, cetearyl alcohol, copernicia cerifera (carnauba) wax, dibutyl adipate, tocopherol (Vitamin E), silica dimethyl silylate, sodium stearoyl glutamate, glyceryl behenate, polyglyceryl-6 octastearate, diethylhexyl syringylidenemalonate, phenoxyethanol, xanthan gum, ethylhexylglycerin, hydroxyacetophenone, disodium EDTA, glycerin, cetyl alcohol, sodium ascorbyl phosphate
- Questions?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
COPPERTONE OIL FREE AND SHINE CONTROL FACE SUNSCREEN SPF 45
avobenzone 3%, homosalate 10%, octisalate 5%, octocrylene 10% lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66800-8164 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g in 100 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 10 g in 100 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 g in 100 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 10 g in 100 g Inactive Ingredients Ingredient Name Strength CARNAUBA WAX (UNII: R12CBM0EIZ) DIBUTYL ADIPATE (UNII: F4K100DXP3) SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024) POLYGLYCERYL-6 ISOSTEARATE (UNII: 5VKGO1O03G) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PHENOXYETHANOL (UNII: HIE492ZZ3T) XANTHAN GUM (UNII: TTV12P4NEE) DISODIUM EDTA-COPPER (UNII: 6V475AX06U) CETYL ALCOHOL (UNII: 936JST6JCN) SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI) ALCOHOL (UNII: 3K9958V90M) ETHYLHEXYLGLYCERYL BEHENATE (UNII: JRY34LRD7B) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) BIS-OCTYLDODECYL DIMER DILINOLEATE/PROPANEDIOL COPOLYMER (UNII: TY3J98ZR7R) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) STARCH, TAPIOCA (UNII: 24SC3U704I) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) TOCOPHEROL (UNII: R0ZB2556P8) DOCOSANOL (UNII: 9G1OE216XY) 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:66800-8164-2 74 g in 1 TUBE; Type 0: Not a Combination Product 01/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/01/2023 Labeler - Beiersdorf Inc (001177906)
