Label: AVBENZONE, HOMOSALATE, OCTISALATE lotion
- NDC Code(s): 79481-0951-1
- Packager: Meijer Distribution, INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 23, 2025
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- 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
- apply to all skin exposed to the sun
- reapply at least every 2 hours
- use a water resistant sunscreen if swimming or sweating
- 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 of age: Ask a doctor
- Other information
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Inactive ingredients
water, C12-15 alkyl benzoate, diethylhexyl 2,6-naphthalate, cetearyl alcohol, glycerin, dimethicone, Glycine soja (soybean) seed extract, phenyl trimethicone, steareth-2, silica, panthenol, laureth-7, arachidyl alcohol, cetearyl glucoside, steareth-21, fragrance, polyacrylamide, behenyl alcohol, C13-14 isoparaffin, chlorphenesin, benzyl alcohol, disodium EDTA, arachidyl glucoside, polymethyl methacrylate, titanium dioxide, mica
- Questions?
- Disclaimers
- Side Panel Claims
- ADVERSE REACTION
- Principal display panel
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INGREDIENTS AND APPEARANCE
AVBENZONE, HOMOSALATE, OCTISALATE
avbenzone, homosalate, octisalate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79481-0951 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 50 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) GLYCERIN (UNII: PDC6A3C0OX) DIMETHICONE (UNII: 92RU3N3Y1O) SOYBEAN (UNII: L7HT8F1ZOD) STEARETH-2 (UNII: V56DFE46J5) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) PANTHENOL (UNII: WV9CM0O67Z) LAURETH-7 (UNII: Z95S6G8201) ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) CHLORPHENESIN (UNII: I670DAL4SZ) BENZYL ALCOHOL (UNII: LKG8494WBH) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ) POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) MICA (UNII: V8A1AW0880) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79481-0951-1 1 in 1 CARTON 08/28/2023 1 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 08/28/2023 Labeler - Meijer Distribution, INC (006959555) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(79481-0951)

