Drug Facts

Drug Labeling and Warnings

Drug Details [pdf]

MAYBELLINE NEW YORK INSTANT AGE REWIND ERASER TREATMENT MAKEUP SPF 18- octinoxate liquid 
L'Oreal USA Products Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Drug Facts

Active ingredient

Octinoxate 7.5%

Directions

Apply before sun exposure.

FOR EXTERNAL USE ONLY. 

When using this product

AVOID CONTACT WITH EYES. 

Discontinue use

IF SIGNS OF IRRITATION OR RASH APPEAR.

Keep out of reach of children.

Not to be swallowed.

Inactive ingredients

WATER
CYCLOPENTASILOXANE
CYCLOHEXASILOXANE
GLYCERIN
BUTYLENE GLYCOL
POLYGLYCERYL-4 ISOSTEARATE
TALC
CETYL PEG/PPG-10/1 DIMETHICONE
HEXYL LAURATE
TRIBEHENIN
DIMETHICONE
PHENYL TRIMETHICONE
MAGNESIUM SULFATE
POLYMETHYLSILSESQUIOXANE
PEG/PPG-18/18 DIMETHICONE
SILICA DIMETHYL SILYLATE
LAURETH-4
DIPHENYL DIMETHICONE
METHYLPARABEN
DIAZOLIDINYL UREA
DISODIUM STEAROYL GLUTAMATE
LYCIUM BARBARUM FRUIT EXTRACT
PROPYLPARABEN
DISTEARDIMONIUM HECTORITE
TOCOPHEROL
CAFFEINE
ALUMINUM HYDROXIDE
ASCORBYL PALMITATE
PROPYLENE GLYCOL
PANTHENOL
ALCOHOL DENAT.
TITANIUM DIOXIDE
MICA

image of a label

MAYBELLINE NEW YORK INSTANT AGE REWIND ERASER TREATMENT MAKEUP SPF 18 
octinoxate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 49967-006
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)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)  
TALC (UNII: 7SEV7J4R1U)  
HEXYL LAURATE (UNII: 4CG9F9W01Q)  
TRIBEHENIN (UNII: 8OC9U7TQZ0)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)  
SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)  
LAURETH-4 (UNII: 6HQ855798J)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
TOCOPHEROL (UNII: R0ZB2556P8)  
CAFFEINE (UNII: 3G6A5W338E)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
ASCORBYL PALMITATE (UNII: QN83US2B0N)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PANTHENOL (UNII: WV9CM0O67Z)  
ALCOHOL (UNII: 3K9958V90M)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
MICA (UNII: V8A1AW0880)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 49967-006-0120 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product10/01/200910/01/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35210/01/200910/01/2014
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
L'Oreal USA Products Inc624244349manufacture(49967-006)

Revised: 12/2018