Label: ESSENCE LIGHT SUNSCREEN SPF 50 PA- avobenzone, homosalate, octisalate, octocrylene lotion
- NDC Code(s): 14268-119-10, 14268-119-50
- Packager: ENGLEWOOD LAB, INC.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 12, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Uses
- Warnings
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Directions
• Apply liberally and evenly 15 minutes before sun exposure • Reapply at least every 2 hours • Use a water-resistant sunscreen if swimming or sweating: • Immediately after towel drying • At least every 2 hours • Children under 6 months of age: Ask a doctor • 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 unscreen 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.
- Other information
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Inactive Ingredients
Water (Aqua), Dipropylene Glycol, Methyl Methacrylate Crosspolymer, Glyceryl Polymethacrylate, Propylene Glycol, Butyloctyl Salicylate, Ceteareth-20, Ethylhexyl Methoxycrylene, Acrylates Copolymer, Galactomyces Ferment Filtrate, Saccharomyces Ferment Filtrate, Ceramide NP, Hydrolyzed Hyaluronic Acid, Sodium Acetylated Hyaluronate, Hyaluronic Acid, Hydrolyzed Sodium Hyaluronate, Sodium Hyaluronate rosspolymer, Potassium Hyaluronate, Panax Ginseng Root Extract, Sorbitan Oleate, Polysorbate 60, Sorbitan Stearate, Caprylyl Glycol, Cetearyl Olivate, Panthenol, Sodium Hyaluronate, Glycerin, Sorbitan Olivate, Acrylates/C10- 30 Alkyl Acrylate Crosspolymer, Tromethamine, Sodium Acrylate/ Sodium Acryloyldimethyl Taurate Copolymer, Isohexadecane, Ammonium Acryloyldimethyltaurate/ VP Copolymer, 1,2-Hexanediol, BHT, Ethylhexylglycerin, Polysorbate 80, Trisodium Ethylenediamine Disuccinate, Xanthan Gum, Butylene Glycol, Caprylic/ Capric Triglyceride, Hydroxypropyltrimonium Hyaluronate, Potassium Sorbate, Hydrogenated Lecithin, Sodium Benzoate, Octyldodecanol
- Package Labeling:10ml
- Package Labeling:50ml
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INGREDIENTS AND APPEARANCE
ESSENCE LIGHT SUNSCREEN SPF 50 PA
avobenzone, homosalate, octisalate, octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:14268-119 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 90 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 45 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 50 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIPROPYLENE GLYCOL (UNII: E107L85C40) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8) CERAMIDE NP (UNII: 4370DF050B) SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93) HYALURONIC ACID (UNII: S270N0TRQY) ASIAN GINSENG (UNII: CUQ3A77YXI) PEG-6 SORBITAN OLEATE (UNII: 58O7V09UCI) SORBITAN MONOOLEATE (UNII: 06XEA2VD56) POLYSORBATE 60 (UNII: CAL22UVI4M) SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CETEARYL OLIVATE (UNII: 58B69Q84JO) PANTHENOL (UNII: WV9CM0O67Z) HYALURONATE SODIUM (UNII: YSE9PPT4TH) GLYCERIN (UNII: PDC6A3C0OX) SORBITAN OLIVATE (UNII: MDL271E3GR) TROMETHAMINE (UNII: 023C2WHX2V) SODIUM ACRYLATE (UNII: 7C98FKB43H) ISOHEXADECANE (UNII: 918X1OUF1E) AMMONIUM ACRYLOYLDIMETHYLTAURATE (UNII: KBC00G95HI) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) POLYSORBATE 80 (UNII: 6OZP39ZG8H) TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q) XANTHAN GUM (UNII: TTV12P4NEE) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM BENZOATE (UNII: OJ245FE5EU) OCTYLDODECANOL (UNII: 461N1O614Y) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:14268-119-50 50 mL in 1 TUBE; Type 0: Not a Combination Product 03/01/2023 2 NDC:14268-119-10 10 mL in 1 TUBE; Type 0: Not a Combination Product 03/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 03/01/2023 Labeler - ENGLEWOOD LAB, INC. (172198223)
