NDC | 49967-406-01, 49967-406-02 |
Set ID | cb523d02-acec-446f-baf5-d38f5a9cf31b |
Category | HUMAN OTC DRUG LABEL |
Packager | L'Oreal USA Products Inc |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- 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 before use
- apply generously 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, dimethicone/PEG-10/15 crosspolymer, sodium chloride, phenoxyethanol, propylene glycol, chlorphenesin, triethoxysilylethyl polydimethylsiloxyethyl dimethicone, isopropyl titanium triisostearate, tocopheryl acetate, fragrance, disodium EDTA, alumina, dipropylene glycol, calendula officinalis flower extract, ruscus aculeatus root exract, sodium hyaluronate, sodium citrate, BHT, benzyl alcohol, tocopherol; may contain: titanium dioxide, iron oxides, bismuth oxychloride
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
YVES SAINT LAURENT TOUCHE ECLAT ALL IN ONE GLOW INSTANT COMPLEXION ENHANCER BROAD SPECTRUM SPF 23 SUNSCREEN
octinoxate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-406 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) SODIUM CHLORIDE (UNII: 451W47IQ8X) PHENOXYETHANOL (UNII: HIE492ZZ3T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CHLORPHENESIN (UNII: I670DAL4SZ) ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) EDETATE DISODIUM (UNII: 7FLD91C86K) ALUMINUM OXIDE (UNII: LMI26O6933) DIPROPYLENE GLYCOL (UNII: E107L85C40) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) RUSCUS ACULEATUS ROOT (UNII: ZW12V95I1Q) HYALURONATE SODIUM (UNII: YSE9PPT4TH) SODIUM CITRATE (UNII: 1Q73Q2JULR) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) BENZYL ALCOHOL (UNII: LKG8494WBH) TOCOPHEROL (UNII: R0ZB2556P8) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERRIC OXIDE RED (UNII: 1K09F3G675) BISMUTH OXYCHLORIDE (UNII: 4ZR792I587) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-406-01 1 in 1 CARTON 12/01/2017 1 30 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:49967-406-02 1 mL in 1 PACKET; Type 0: Not a Combination Product 12/01/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 12/01/2017 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations SICOS ET CIE 276993581 manufacture(49967-406) , pack(49967-406) Establishment Name Address ID/FEI Business Operations Socoplan 276221405 pack(49967-406)