Label: SKINCEUTICALS LIGHT MOISTURE UV DEFENSE BROAD SPECTRUM SPF 50 SUNSCREEN- avobenzone, homosalate, octisalate and octocrylene lotion
- NDC Code(s): 49967-888-01, 49967-888-02
- Packager: L'Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 28, 2023
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
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Directions
For sunscreen use:
● apply liberally 15 minutes before sun exposure
● reapply at least every 2 hours
● use a water resistant sunscreen if swimming or sweating
● 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
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Inactive ingredients
dwater, styrene/acrylates copolymer, dimethicone, polymethylsilsesquioxane, butyloctyl salicylate,
glycerin, alcohol denat., poly c10-30 alkyl acrylate, caprylyl methicone, trisiloxane, acrylates/c10-30 alkyl acrylate crosspolymer, acrylates/dimethicone copolymer, caprylic/capric triglyceride, caprylyl glycol, diethylhexyl, syringylidenemalonate, disodium EDTA, glyceryl stearate, inulin lauryl carbamate, p-anisic acid, PEG-100 stearate, PEG-8 laurate, phenoxyethanol, potassium cetyl phosphate, tocopherol, triethanolamine, xanthan gum - Questions or comments?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SKINCEUTICALS LIGHT MOISTURE UV DEFENSE BROAD SPECTRUM SPF 50 SUNSCREEN
avobenzone, homosalate, octisalate and octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-888 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) STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A) DIMETHICONE (UNII: 92RU3N3Y1O) POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) GLYCERIN (UNII: PDC6A3C0OX) ALCOHOL (UNII: 3K9958V90M) CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL) TRISILOXANE (UNII: 9G1ZW13R0G) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CAPRYLYL GLYCOL (UNII: 00YIU5438U) DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) P-ANISIC ACID (UNII: 4SB6Y7DMM3) PEG-100 STEARATE (UNII: YD01N1999R) PEG-8 LAURATE (UNII: 762O8IWA10) PHENOXYETHANOL (UNII: HIE492ZZ3T) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) TOCOPHEROL (UNII: R0ZB2556P8) TROLAMINE (UNII: 9O3K93S3TK) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-888-01 1 in 1 CARTON 03/01/2018 09/22/2025 1 200 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:49967-888-02 1 in 1 CARTON 03/01/2018 09/22/2025 2 4 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 OTC Monograph Drug M020 03/01/2018 09/22/2025 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations Cosmetic Essence, LLC 032565959 manufacture(49967-888)