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 August 29, 2024
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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 {and evenly} 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?
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Disclaimer
May stain or damage some fabrics or surfaces
* This product is not manufactured or distributed by Johnson & Johnson Corporation, distributor of Aveeno® Postively Radiant® Daily Moisturizer Sunscreen Broad spectrum SPF 15
This light, fast absorbing moisturizer helps even out the appearance of skin tone and texture by subtly reflecting light to immediately enhance your skin's appearance.
- SPL UNCLASSIFIED SECTION
- 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)