MAYBELLINE NEW YORK INSTANT AGE REWIND ERASER TREATMENT MAKEUP OCTINOXATE BROAD SPECTRUM SPF 20 SUNSCREEN PLUS PROVITAMIN B5- octinoxate lotion 
L'Oreal USA Products Inc

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Drug Facts

Active ingredient

Octinoxate 7.5%

Purpose

Sunscreen

Uses

Warnings

For external use only

Do not use

on damaged or broken skin

When using this product

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

rash occurs

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

For sunscreen use:

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

Questions or comments?

1-800-322-2036

Monday - Friday (9 a.m. - 5 p.m. EST)

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MAYBELLINE NEW YORK INSTANT AGE REWIND ERASER TREATMENT MAKEUP OCTINOXATE BROAD SPECTRUM SPF 20 SUNSCREEN PLUS PROVITAMIN B5 
octinoxate lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-202
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Octinoxate (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) Octinoxate75 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-202-0120 mL in 1 BOTTLE; Type 0: Not a Combination Product01/14/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02001/14/2024
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
L'OREAL USA PRODUCTS, INC624244349manufacture(49967-202)

Revised: 6/2024
Document Id: e4c50d8c-3ab1-4281-bd1a-34e90549ac30
Set id: 12ec5a93-8c24-4ac9-94df-910dd8137e00
Version: 1
Effective Time: 20240627
 
L'Oreal USA Products Inc