Label: COPPERTONE EVERYTONE SUNSCREEN SPF 50- avobenzone 3%, homosalate 9%, octisalate 4.5%, octocrylene 9% spray
- NDC Code(s): 66800-5049-5
- Packager: Beiersdorf Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 17, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients
- Purpose
- Use
- Warnings
- DO NOT USE
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WHEN USING
When using this product
■ keep away from face to avoid breathing it■ keep out of eyes. Rinse with water to remove.
■ use only as directed. Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.
■ do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120˚F.
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
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Directions
■ shake well before each use
■ spray liberally and spread evenly by hand 15 minutes before sun exposure
■ hold container 4 to 6 inches from the skin to apply
■ do not spray directly into face. Spray on hands then apply to face.
■ do not apply in windy conditions
■ use in a well-ventilated area
■ 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, isobutane, SD alcohol 40-B (7.1% v/v), butyloctyl salicylate, diethylhexyl carbonate, glycereth-26, styrene/acrylates copolymer, butylene glycol, diisopropyl adipate, dimethicone, polyamide-8, isododecane, 1,2-hexanediol, ammonium acryloyldimethyltaurate/beheneth-25 methacrylate crosspolymer, glycerin, aloe barbadensis leaf juice, tocopherol (vitamin E), sodium ascorbyl phosphate, hydroxyacetophenone, ethylhexyl methoxycrylene, arachidyl alcohol, xanthan gum, behenyl alcohol, arachidyl glucoside, disodium EDTA
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INGREDIENTS AND APPEARANCE
COPPERTONE EVERYTONE SUNSCREEN SPF 50
avobenzone 3%, homosalate 9%, octisalate 4.5%, octocrylene 9% sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66800-5049 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 4.5 g in 100 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 9 g in 100 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 g in 100 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 9 g in 100 g Inactive Ingredients Ingredient Name Strength XANTHAN GUM (UNII: TTV12P4NEE) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) GLYCERETH-26 (UNII: NNE56F2N14) ALOE VERA LEAF (UNII: ZY81Z83H0X) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) DOCOSANOL (UNII: 9G1OE216XY) ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ) WATER (UNII: 059QF0KO0R) SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR) ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8) ALCOHOL (UNII: 3K9958V90M) DIETHYLHEXYL CARBONATE (UNII: YCD50O0Z6L) ISODODECANE (UNII: A8289P68Y2) ISOBUTANE (UNII: BXR49TP611) STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A) DIMETHICONE (UNII: 92RU3N3Y1O) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) AMMONIUM ACRYLOYLDIMETHYLTAURATE/BEHENETH-25 METHACRYLATE CROSSPOLYMER (52000 MPA.S) (UNII: LZ291VH90H) GLYCERIN (UNII: PDC6A3C0OX) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) DISODIUM EDTA-COPPER (UNII: 6V475AX06U) POLYAMIDE-8 (4500 MW) (UNII: 77723GV81A) ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU) DIISOPROPYL ADIPATE (UNII: P7E6YFV72X) TOCOPHEROL (UNII: R0ZB2556P8) Product Characteristics Color white (clear to white) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66800-5049-5 142 g in 1 CAN; Type 0: Not a Combination Product 11/03/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 11/03/2023 Labeler - Beiersdorf Inc (001177906)