Label: GARNIER OMBRELLE ULTRA LIGHT ADVANCED BROAD SPECTRUM SPF 60 SUNSCREEN- drometrizole trisiloxane, bemotrizinol, octisalate, octocrylene, avobenzone, homosalate and ensulizole lotion
- NDC Code(s): 49967-649-01
- Packager: L'Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated June 27, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor
- Keep out of reach of children.
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Directions
Adults and adolescents 12 to 17 years.
- Apply generously and evenly 15 minutes before sun exposure
- Reapply at least every 2 hours
- Reapply after 80 minutes of siwmming or sweating
- Reapply immediately after towel drying
- 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 Broad Spectrum SPF 15 or higher sunscreen
- limit time in the sun, especially from 10 a.m. - 2 p.m.
- wear long-sleeved shirts, pants, hats, and sunglasses.
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Inactive ingredients
water, alcohol denat., silica, , isopropyl myristate, glycerin, diisopropyl sebacate, propanediol, c12-22 alkyl acrylate/hydroxyethylacrylate copolymer, perlite, dl-alpha tocopherol, triethanolamine, caprylyl glycol, trisodium ethylenediamine disuccinate, hydroxyethylcellulose, acrylate/c10-30 alkyl acrylate crosspolymer, pentylene glycol, butylene glycol, citric acid
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INGREDIENTS AND APPEARANCE
GARNIER OMBRELLE ULTRA LIGHT ADVANCED BROAD SPECTRUM SPF 60 SUNSCREEN
drometrizole trisiloxane, bemotrizinol, octisalate, octocrylene, avobenzone, homosalate and ensulizole lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-649 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DROMETRIZOLE TRISILOXANE (UNII: HC22845I1X) (DROMETRIZOLE TRISILOXANE - UNII:HC22845I1X) DROMETRIZOLE TRISILOXANE 70 mg in 1 mL BEMOTRIZINOL (UNII: PWZ1720CBH) (BEMOTRIZINOL - UNII:PWZ1720CBH) BEMOTRIZINOL 50 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 AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 20 mg in 1 mL ENSULIZOLE (UNII: 9YQ9DI1W42) (ENSULIZOLE - UNII:9YQ9DI1W42) ENSULIZOLE 5 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) GLYCERIN (UNII: PDC6A3C0OX) DIISOPROPYL SEBACATE (UNII: J8T3X564IH) PROPANEDIOL (UNII: 5965N8W85T) PERLITE (UNII: 0SG101ZGK9) .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01) TROLAMINE (UNII: 9O3K93S3TK) CAPRYLYL GLYCOL (UNII: 00YIU5438U) TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q) HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V) PENTYLENE GLYCOL (UNII: 50C1307PZG) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-649-01 1 in 1 CARTON 02/01/2023 1 50 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date export only 02/01/2023 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'OREAL USA PRODUCTS, INC 624244349 manufacture(49967-649)