Label: LA ROCHE POSAY ANTHELIOS SUNSCREEN SPF 60 ULTRA LIGHT- avobenzone, homosalate, octisalate, octocrylene, oxybenzone spray
- NDC Code(s): 82046-692-01
- Packager: L'Oreal USA, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 21, 2023
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- Drug Facts
- Active ingredients
- Uses
- Warnings
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Directions
For sunscreen use:
- spray generously and spread evenly by hand 15 minutes before sun exposure
- hold container 4 to 6 inches from 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
- Spending time in the sun increases your risk of skin cancer and early skin aging. To decreases this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: Sun Protection Measures.
- 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, dimethicone, isopropyl lauroyl sarcosinate, glycerin, styrene/acrylates copolymer, isotridecyl isononanoate, polyurethane-35, caprylyl methicone, octyldodecanol, phenoxyethanol, propylene glycol, caprylyl glycol, sodium stearoyl glutamate, polysorbate 61, glyceryl stearate, PEG-8 laurate, dimethiconol, octyldodecyl xyloside, PEG-12 dimethicone, p-anisic acid, stearyl alcohol, disodium EDTA, tocopherol, diethylhexyl syringylidenemalonate, cassia alata leaf extract, maltodextrin
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INGREDIENTS AND APPEARANCE
LA ROCHE POSAY ANTHELIOS SUNSCREEN SPF 60 ULTRA LIGHT
avobenzone, homosalate, octisalate, octocrylene, oxybenzone sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82046-692 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 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 96 mg in 1 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 29 mg in 1 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 54 mg in 1 g OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 35 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) ISOPROPYL LAUROYL SARCOSINATE (UNII: LYR06W430J) GLYCERIN (UNII: PDC6A3C0OX) ISOTRIDECYL ISONONANOATE (UNII: WEF51750MT) CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL) OCTYLDODECANOL (UNII: 461N1O614Y) PHENOXYETHANOL (UNII: HIE492ZZ3T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CAPRYLYL GLYCOL (UNII: 00YIU5438U) SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024) POLYSORBATE 61 (UNII: X9E1MY2JQG) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PEG-8 LAURATE (UNII: 762O8IWA10) OCTYLDODECYL XYLOSIDE (UNII: 8Z6VNR46QM) PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95) P-ANISIC ACID (UNII: 4SB6Y7DMM3) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) TOCOPHEROL (UNII: R0ZB2556P8) DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248) SENNA ALATA LEAF (UNII: 4BXR6YZN92) MALTODEXTRIN (UNII: 7CVR7L4A2D) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82046-692-01 143 g in 1 CAN; Type 0: Not a Combination Product 01/01/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/01/2014 Labeler - L'Oreal USA, Inc. (002136794)
