Label: GARNIER OMBRELLE ULTRA LIGHT ADVANCED 30- avobenzone, homosalate, octisalate, octocrylene and oxybenzone/ lotion
- NDC Code(s): 49967-656-01
- Packager: L'OREAL USA PRODUCTS INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Export only
Drug Label Information
Updated January 31, 2024
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- Active ingredients
- Warnings
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Inactive ingredients
water, cyclopentasiloxane, dicaprylyl ether, alcohol denat., silica, dimethicone, styrene/acrylates copolymer, PEG-30 dipolyhydroxystearate, cyclohexasiloxane, polymethylsilsesquioxane, nylon-12, dicaprylyl carbonate, phenoxyethanol, lauryl PEG/PPG-18/18 methicone, sodium chloride, caprylyl glycol, PEG-8 laurate, methylparaben, poly c10-30 alkyl acrylate, disteardimonium hectorite, isostearyl alcohol. disodium EDTA, dodecane, poloxamer 407, tocopherol, sodium dodecylbenzenesulfonate
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INGREDIENTS AND APPEARANCE
GARNIER OMBRELLE ULTRA LIGHT ADVANCED 30
avobenzone, homosalate, octisalate, octocrylene and oxybenzone/ lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-656 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 50 mg in 1 mL OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 30 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) ALCOHOL (UNII: 3K9958V90M) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) DICAPRYLYL ETHER (UNII: 77JZM5516Z) STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A) PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO) DIMETHICONE (UNII: 92RU3N3Y1O) CYCLOMETHICONE 6 (UNII: XHK3U310BA) POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69) NYLON-12 (UNII: 446U8J075B) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) PHENOXYETHANOL (UNII: HIE492ZZ3T) LAURYL PEG/PPG-18/18 METHICONE (UNII: ZJ5S27D9NX) SODIUM CHLORIDE (UNII: 451W47IQ8X) CAPRYLYL GLYCOL (UNII: 00YIU5438U) PEG-8 LAURATE (UNII: 762O8IWA10) METHYLPARABEN (UNII: A2I8C7HI9T) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) ISOSTEARYL ALCOHOL (UNII: Q613OCQ44Y) EDETATE DISODIUM (UNII: 7FLD91C86K) DODECENE (UNII: WYE669F3GR) POLOXAMER 407 (UNII: TUF2IVW3M2) TOCOPHEROL (UNII: R0ZB2556P8) SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-656-01 1 in 1 CARTON 02/01/2015 10/30/2024 1 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 export only 02/01/2015 10/30/2024 Labeler - L'OREAL USA PRODUCTS INC (002136794) Establishment Name Address ID/FEI Business Operations L'OREAL USA, INC 624244349 manufacture(49967-656) , pack(49967-656)