Label: LANCOME PARIS SKIN FEELS GOOD BROAD SPECTRUM SPF 23 SUNSCREEN HYDRATING SKIN TINT HEALTHY GLOW- octinoxate liquid
- NDC Code(s): 49967-736-01, 49967-736-02
- Packager: L'Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 23, 2023
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- Flammable until dry.
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
-
Directions
For sunscreen use:
● shake well
● 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
-
Inactive ingredients
water, glycerin, caprylyl methicone, propanediol, dimethicone, rosa gallica flower exract, sorbitol, triethoxysilylethyl polydimethylsiloxyethyl dimethicone, dimethicone/PEG-10/15 crosspolymer, sodium chloride, sodium citrate, sodium hyaluronate, morninga oleifera seed extract, alumina, disodium EDTA, disodium phosphate, isopropyl titanium triisostearate, propylene glycol, diproplylene glycol, citric acid, BHT, tocopherol, phenoxyethanol, chlorphenesin, fragrance; may contain: titanium dioxide, iron oxides
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- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LANCOME PARIS SKIN FEELS GOOD BROAD SPECTRUM SPF 23 SUNSCREEN HYDRATING SKIN TINT HEALTHY GLOW
octinoxate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-736 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Octinoxate (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) Octinoxate 30 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL) PROPANEDIOL (UNII: 5965N8W85T) DIMETHICONE (UNII: 92RU3N3Y1O) ROSA GALLICA FLOWER (UNII: X8W61WUV70) SORBITOL (UNII: 506T60A25R) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM CITRATE (UNII: 1Q73Q2JULR) HYALURONATE SODIUM (UNII: YSE9PPT4TH) MORINGA OLEIFERA LEAF (UNII: 4WET1AWO9B) ALUMINUM OXIDE (UNII: LMI26O6933) EDETATE DISODIUM (UNII: 7FLD91C86K) SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) DIPROPYLENE GLYCOL (UNII: E107L85C40) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) TOCOPHEROL (UNII: R0ZB2556P8) PHENOXYETHANOL (UNII: HIE492ZZ3T) CHLORPHENESIN (UNII: I670DAL4SZ) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERRIC OXIDE RED (UNII: 1K09F3G675) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-736-01 1 in 1 CARTON 11/01/2017 1 32 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:49967-736-02 4 mL in 1 PACKET; Type 0: Not a Combination Product 11/01/2017 11/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 11/01/2017 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations SICOS ET CIE 276993581 manufacture(49967-736) , pack(49967-736)
