NDC | 49967-939-01 |
Set ID | 15470314-70a2-4411-9530-3a59f9d0a66d |
Category | HUMAN OTC DRUG LABEL |
Packager | L'Oreal USA Products Inc |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- 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.
-
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 of 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, dimethicone, alcohol denat., aloe barbadensis leaf juice, phenoxyethanol, caprylyl glycol, sodium polyacrylate, silica, acrylates/c10-30 alkyl acrylate crosspolymer, tocopherol, ascorbyl glucoside, fragrance, sodium hyaluronate, menthyl lactate, disodium EDTA, sodium hydroxide, lycium barbarum fruit extract, limonene, ceramide 3, linalool, sodium benzoate, citronellol, lactic acid, potassium sorbate, geraniol, citric acid, benzyl alcohol, benzyl salicylate, punica granatum extract
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
GARNIER SKINACTIVE MOISTURE BOMB BROAD SPECTRUM SPF 30 SUNSCREEN
avobenzone, homosalate, octisalate, octocrylene and oxybenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-939 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX) Avobenzone 22 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 80 mg in 1 mL Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate 24 mg in 1 mL Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM) Octocrylene 45 mg in 1 mL OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 29 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) DIMETHICONE (UNII: 92RU3N3Y1O) ALCOHOL (UNII: 3K9958V90M) ALOE VERA LEAF (UNII: ZY81Z83H0X) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) TOCOPHEROL (UNII: R0ZB2556P8) ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW) HYALURONATE SODIUM (UNII: YSE9PPT4TH) MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I) EDETATE DISODIUM (UNII: 7FLD91C86K) SODIUM HYDROXIDE (UNII: 55X04QC32I) LYCIUM BARBARUM FRUIT (UNII: 930626MWDL) LIMONENE, (+)- (UNII: GFD7C86Q1W) CERAMIDE 3 (UNII: 4370DF050B) LINALOOL, (+/-)- (UNII: D81QY6I88E) SODIUM BENZOATE (UNII: OJ245FE5EU) .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K) LACTIC ACID (UNII: 33X04XA5AT) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) GERANIOL (UNII: L837108USY) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) BENZYL ALCOHOL (UNII: LKG8494WBH) BENZYL SALICYLATE (UNII: WAO5MNK9TU) PUNICA GRANATUM ROOT BARK (UNII: CLV24I3T1D) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-939-01 1 in 1 CARTON 01/01/2017 1 75 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 not final part352 01/01/2017 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'Oreal USA, Inc. 624244349 manufacture(49967-939)