Label: MAYBELLINE NEW YORK INSTANT AGE REWIND ERASER TREATMENT MAKEUP OCTINOXATE BROAD SPECTRUM SPF 20 SUNSCREEN PLUS PROVITAMIN B5- octinoxate lotion
- NDC Code(s): 49967-202-01
- Packager: L'Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 27, 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 sunscren if swimming or sweating
- Sun Protection Measures. Spending time in the sun increases our 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
cyclopentasiloxane, water, dimethicone crosspolymer, glycerin, isotridecyl isononanoate, PEG-9 polydimethylsiloxyethyl dimethicone, disteardimonium hectorite, phenoxyethanol, PEG-10 dimethicone, hydrolyzed wheat protein/pvp crosspolymer, disodium stearoyl glutamate, chlorphenesin, methylparaben, lycium barbarum fruit extract, silica silylate, potassium sorbate, ethylparaben, tocopherol, ascorbyl palmitate, panthenol, aluminum hydroxide, citric acid, BHT, sodium PCA, propylene glycol, urea, EDTA, tin oxide, ethylhexylglycerin, trehalose, polyquaternium-51, soluble collagen, sodium hyaluronate, trisodium EDTA, benzoic acid; may contain: titanium dioxide, mica, iron oxides
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- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MAYBELLINE NEW YORK INSTANT AGE REWIND ERASER TREATMENT MAKEUP OCTINOXATE BROAD SPECTRUM SPF 20 SUNSCREEN PLUS PROVITAMIN B5
octinoxate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-202 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Octinoxate (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) Octinoxate 75 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) ISOTRIDECYL ISONONANOATE (UNII: WEF51750MT) PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: TYP81E471F) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) PHENOXYETHANOL (UNII: HIE492ZZ3T) DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M) CHLORPHENESIN (UNII: I670DAL4SZ) METHYLPARABEN (UNII: A2I8C7HI9T) LYCIUM BARBARUM FRUIT (UNII: 930626MWDL) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) ETHYLPARABEN (UNII: 14255EXE39) TOCOPHEROL (UNII: R0ZB2556P8) ASCORBYL PALMITATE (UNII: QN83US2B0N) PANTHENOL (UNII: WV9CM0O67Z) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) UREA (UNII: 8W8T17847W) EDETIC ACID (UNII: 9G34HU7RV0) STANNIC OXIDE (UNII: KM7N50LOS6) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) TREHALOSE (UNII: B8WCK70T7I) HYALURONATE SODIUM (UNII: YSE9PPT4TH) EDETATE TRISODIUM (UNII: 420IP921MB) BENZOIC ACID (UNII: 8SKN0B0MIM) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) MICA (UNII: V8A1AW0880) FERRIC OXIDE RED (UNII: 1K09F3G675) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-202-01 20 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/14/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/14/2024 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'OREAL USA PRODUCTS, INC 624244349 manufacture(49967-202)