Label: COPPERTONE GLOW SUNCREEN SPF 30- avobenzone, homosalate, octisalate, octocrylene aerosol, spray
- NDC Code(s): 66800-0003-5
- Packager: Beiersdord Inc
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated January 9, 2024
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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
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
Inactive ingredients water, isobutane, SD alcohol 40-B (12.6% v/v), diethylhexyl carbonate, butyloctyl salicylate, diisopropyl adipate, glycereth-26, butylene glycol, dimethicone, polyamide-8, isododecane, styrene/acrylates copolymer, 1,2-hexanediol, ammonium acryloyldimethyltaurate/beheneth-25 methacrylate crosspolymer, glycerin, hydroxyacetophenone, mica, synthetic fluorphlogopite, tocopherol, ethylhexyl methoxycrylene, arachidyl alcohol, iron oxides, bismuth oxychloride, fragrance, xanthan gum, behenyl alcohol, silica, arachidyl glucoside, disodium EDTA, sodium ascorbyl phosphate
- Questions
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INGREDIENTS AND APPEARANCE
COPPERTONE GLOW SUNCREEN SPF 30
avobenzone, homosalate, octisalate, octocrylene aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66800-0003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 80 mg in 1 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 90 mg in 1 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 45 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR) ISOBUTANE (UNII: BXR49TP611) GLYCERETH-26 (UNII: NNE56F2N14) DOCOSANOL (UNII: 9G1OE216XY) FRAGRANCE FRESH CITRUS FLORAL ORC1501495 (UNII: OU4GI2R2WB) STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) AMMONIUM ACRYLOYLDIMETHYLTAURATE/BEHENETH-25 METHACRYLATE CROSSPOLYMER (52000 MPA.S) (UNII: LZ291VH90H) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) POLYAMIDE-8 (4500 MW) (UNII: 77723GV81A) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) DIETHYLHEXYL CARBONATE (UNII: YCD50O0Z6L) MAGNESIUM POTASSIUM ALUMINOSILICATE FLUORIDE (UNII: YK3DC63Y5M) TOCOPHEROL (UNII: R0ZB2556P8) ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8) DIISOPROPYL ADIPATE (UNII: P7E6YFV72X) ISODODECANE (UNII: A8289P68Y2) GLYCERIN (UNII: PDC6A3C0OX) DIMETHICONE (UNII: 92RU3N3Y1O) COBALT DISODIUM EDETATE (UNII: 3EY1Y2QRLI) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ) ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU) MICA (UNII: V8A1AW0880) XANTHAN GUM (UNII: TTV12P4NEE) ALCOHOL (UNII: 3K9958V90M) BISMUTH OXYCHLORIDE (UNII: 4ZR792I587) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) Product Characteristics Color white (White to Pale Yellow) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66800-0003-5 142 g in 1 CAN; Type 0: Not a Combination Product 11/02/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 11/02/2020 Labeler - Beiersdord Inc (001177906)