Label: CVS HEALTH SPORT SPF 50- avobenzone, homosalate, octisalate, octocrylene lotion
- NDC Code(s): 51316-037-11
- Packager: CVS PHARMACY
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated March 23, 2023
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask doctor if
- 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
- children under 6 months of age: Ask a doctor
- 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
- Other information
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Inactive ingredients
WATER, GLYCERYL STEARATE, PEG-100 STEARATE, CETYL ALCOHOL, CETYL DIMETHICONE, PROPYLENE GLYCOL, PHENOXYETHANOL, CAPRYLYL GLYCOL, VP/EICOSENE COPOLYMER, ACRYLATES/C12-22 ALKYL METHACRYLATE COPOLYMER, BEHENYL ALCOHOL, SODIUM POLYACRYLATE, CHLORPHENESIN, XANTHAN GUM, DISODIUM EDTA, FRAGRANCE, TOCOPHERYL ACETATE, ALOE BARBADENSIS LEAF JUICE
- Label
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INGREDIENTS AND APPEARANCE
CVS HEALTH SPORT SPF 50
avobenzone, homosalate, octisalate, octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51316-037 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 27 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 90 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 45 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 65 mg in 1 mL Inactive Ingredients Ingredient Name Strength .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) EICOSYL POVIDONE (UNII: XQQ9MKE2BJ) DOCOSANOL (UNII: 9G1OE216XY) ALOE VERA LEAF (UNII: ZY81Z83H0X) PEG-100 STEARATE (UNII: YD01N1999R) GLYCERYL 1-STEARATE (UNII: 258491E1RZ) CETYL ALCOHOL (UNII: 936JST6JCN) BUTYL ACRYLATE/C16-C20 ALKYL METHACRYLATE/METHACRYLIC ACID/METHYL METHACRYLATE COPOLYMER (UNII: 7K68DGG29P) DIMETHICONE (UNII: 92RU3N3Y1O) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CHLORPHENESIN (UNII: I670DAL4SZ) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) EDETATE DISODIUM (UNII: 7FLD91C86K) CETYL DIMETHICONE 45 (UNII: IK315POC44) PHENOXYETHANOL (UNII: HIE492ZZ3T) WATER (UNII: 059QF0KO0R) XANTHAN GUM (UNII: TTV12P4NEE) SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51316-037-11 237 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/10/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M020 11/10/2021 Labeler - CVS PHARMACY (062312574)
