Label: EQUATE SUNSCREEN SPORT SPF 100- avobenzone homosalate octisalate octocrylene oxybenzone lotion
- NDC Code(s): 49035-789-15
- Packager: Walmart Stores Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 December 21, 2022
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- When using this product
- Do not use
- Stop use and ask a 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
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
• children under 6 months: Ask a doctor
- Other information
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Inactive ingredients
water, propylene glycol, styrene/acrylates copolymer, behenyl alcohol, glyceryl stearate, microcrystalline cellulose, benzyl alcohol, myristyl alcohol, stearic acid, hydrolyzed wheat protein/PVP crosspolymer, lauryl alcohol, cetyl alcohol, tocopherol (vitamin E), sodium ascorbyl phosphate (vitamin C phosphate), lecithin, cellulose gum, fragrance, butylated PVP, disodium EDTA, caprylyl glycol, ethylhexyl glycerin, phenoxyethanol
- Label
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INGREDIENTS AND APPEARANCE
EQUATE SUNSCREEN SPORT SPF 100
avobenzone homosalate octisalate octocrylene oxybenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-789 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 150 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 100 mg in 1 mL OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 60 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) BENZYL ALCOHOL (UNII: LKG8494WBH) MYRISTYL ALCOHOL (UNII: V42034O9PU) STEARIC ACID (UNII: 4ELV7Z65AP) HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL) LAURYL ALCOHOL (UNII: 178A96NLP2) CETYL ALCOHOL (UNII: 936JST6JCN) .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01) SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) CAPRYLYL GLYCOL (UNII: 00YIU5438U) EDETATE DISODIUM (UNII: 7FLD91C86K) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PHENOXYETHANOL (UNII: HIE492ZZ3T) DOCOSANOL (UNII: 9G1OE216XY) CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-789-15 177 mL in 1 TUBE; Type 0: Not a Combination Product 11/08/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 11/08/2017 Labeler - Walmart Stores Inc. (051957769)