Label: GARNIER GREEN LABS PORE PERFECTING CANNAB SERUM BROAD SPECTRUM SPF 30 SUNSCREEN- avobenzone, homosalate, octisalate and octocrylene cream
- NDC Code(s): 49967-260-01
- Packager: L’Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 1, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
-
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
water, glycerin, dimethicone, silica, niacinamide, cannabis sativa seed oil, PEG-100 stearate, glyceryl stearate, dicaprylyl carbonate, tocopherol, sodium hydroxide, stearic acid, phenoxyethanol, steareth-100, palmitic acid, ammonium polyacryloyldimethyl taurate, dimethicone/vinyl dimethicone crosspolymer, xanthan gum, capryloyl salicylic acid, caprylyl glycol, myristic acid, disodium EDTA, fragrance
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- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
GARNIER GREEN LABS PORE PERFECTING CANNAB SERUM BROAD SPECTRUM SPF 30 SUNSCREEN
avobenzone, homosalate, octisalate and octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-260 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 50 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 72 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) DIMETHICONE (UNII: 92RU3N3Y1O) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) NIACINAMIDE (UNII: 25X51I8RD4) CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S) PEG-100 STEARATE (UNII: YD01N1999R) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) TOCOPHEROL (UNII: R0ZB2556P8) SODIUM HYDROXIDE (UNII: 55X04QC32I) STEARIC ACID (UNII: 4ELV7Z65AP) PHENOXYETHANOL (UNII: HIE492ZZ3T) STEARETH-100 (UNII: 4OH5W9UM87) PALMITIC ACID (UNII: 2V16EO95H1) AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (55000 MPA.S) (UNII: F01RIY4371) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) XANTHAN GUM (UNII: TTV12P4NEE) CAPRYLOYL SALICYLIC ACID (UNII: 5F7PJF6AA4) CAPRYLYL GLYCOL (UNII: 00YIU5438U) MYRISTIC ACID (UNII: 0I3V7S25AW) EDETATE DISODIUM (UNII: 7FLD91C86K) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-260-01 1 in 1 CARTON 08/01/2020 1 72 mL in 1 BOTTLE, PUMP; 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 08/01/2020 Labeler - L’Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L’Oreal USA, Inc. 624244349 manufacture(49967-260) , pack(49967-260)
