Label: LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS 60 FACE LIGHT FLUID SUNSCREEN BROAD SPECTRUM SPF 60 WATER RESISTANT 80 MINUTES- avobenzone, homosalate, octisalate and octocrylene lotion
- NDC Code(s): 69625-496-01, 69625-496-02, 69625-496-03
- Packager: Cosmetique Active Production
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 31, 2024
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Flammable until dry.
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
-
Directions
For sunscreen use:
- shake well before use
- apply generously 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 of age: Ask a doctor
- Other information
-
Inactive ingredients
water, cyclopentasiloxane, alcohol denat., silica, dicaprylyl ether, styrene/acrylates copolymer, PEG-30 dipolyhydroxystearate, dimethicone, cyclohexasiloxane, polymethylsilsesquioxane, nylon-12, dicaprylyl carbonate, diethylhexyl syringlyidenemalonate, phenoxyethanol, lauryl PEG/PPG-18/18 methicone, sodium chloride, caprylyl glycol, PEG-8 laurate, isostearyl alcohol, poly C10-30 alkyl acrylate, disteardimonium hectorite, p-anisic acid, caprylic/capric triglyceride, disodium EDTA, cassia alata leaf extract, maltodextrin, propylene carbonate, sodium dodecylbenzenesulfonate, tocopherol
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- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS 60 FACE LIGHT FLUID SUNSCREEN BROAD SPECTRUM SPF 60 WATER RESISTANT 80 MINUTES
avobenzone, homosalate, octisalate and octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69625-496 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 100 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 70 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6) ALCOHOL (UNII: 3K9958V90M) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) DICAPRYLYL ETHER (UNII: 77JZM5516Z) STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A) PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO) DIMETHICONE (UNII: 92RU3N3Y1O) CYCLOMETHICONE 6 (UNII: XHK3U310BA) POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK) NYLON-12 (UNII: 446U8J075B) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248) PHENOXYETHANOL (UNII: HIE492ZZ3T) LAURYL PEG/PPG-18/18 METHICONE (UNII: ZJ5S27D9NX) SODIUM CHLORIDE (UNII: 451W47IQ8X) CAPRYLYL GLYCOL (UNII: 00YIU5438U) PEG-8 LAURATE (UNII: 762O8IWA10) ISOSTEARYL ALCOHOL (UNII: Q613OCQ44Y) STEARYL ACRYLATE POLYMER (110000 MW) (UNII: N85XDY2F7W) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) P-ANISIC ACID (UNII: 4SB6Y7DMM3) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) SENNA ALATA LEAF (UNII: 4BXR6YZN92) MALTODEXTRIN (UNII: 7CVR7L4A2D) PROPYLENE CARBONATE (UNII: 8D08K3S51E) SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y) TOCOPHEROL (UNII: R0ZB2556P8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69625-496-01 1 in 1 CARTON 05/01/2020 05/01/2020 1 50 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:69625-496-02 1 in 1 CARTON 05/01/2020 2 5 mL in 1 TUBE; Type 0: Not a Combination Product 3 NDC:69625-496-03 1 in 1 CARTON 05/01/2020 3 50 mL in 1 BOTTLE; 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 05/01/2020 Labeler - Cosmetique Active Production (282658798) Establishment Name Address ID/FEI Business Operations Cosmetique Active Production 282658798 manufacture(69625-496) , analysis(69625-496) , pack(69625-496) Establishment Name Address ID/FEI Business Operations Interspray 364829903 pack(69625-496)
