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Recover Lightening Complex

Generic Name: hydroquinone
Dosage Form: lotion

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Active Ingredient: 4% HYDROQUINONE

gently smooth over entire face. Let product absorb at least 2 minutes before applying lotion.

Gently smooth over entire face. Let product absorb at least 2 minutes before applying lotion.

For external use only. When using this product avoid contact with eyes. If contact occurs, flush throughly with water. Keep out of the reach of children. If swallowed get medical help or contact Poison Control Center right away.

WATER, ETHANOL SD 39C, POLYETHYLENE, SODIUM POLYACRYLATE , PPG-3 BENZYL ETHER 2 ETHYLHEXANOATE, POLYACRYLAMIDE, C13- 14 ISOPARAFIN, LAURETH-7, GLYCERIN, BUTYLENE GLYCOL, PENTYLENE GLYCOL, HYDROXYPHENYL PROPAMIDOBENZOIC ACID, TRIETHANOLAMINE, UNDECYLENOYL PHENYLALANINE, SODIUM PALMITOYL PROLINE, NUMPHAEA ALBA FLOWER EXTRACT, GLYCOLIC ACID, BISABOLOL, ZINGIBER OFFICINALE (GINGER) ROOT EXTRACT, PHENOXYETHANOL, CAPRYLYL GLYCOL, POTASSIUM SORBATE, HEXYLENE GLYCOL, DIMETHYLMETHOXY CHROMANYL PALMITATE, DISODIUM EDTA, SODIUM METABISULFITE, FRAGRANCE

This lightening treatment lightens the skin with minimal irritation. Brightens sun damage, Melasma and dark spots on skin.

This lightening treatment lightens skin with minimal irritation. Brightens sun damage, Melasma and dark spots on skin.

Keep out of reach of children. If swallowed get medial help or contact Poison Control Center right away.

Recover Lightening Complex WITH 4% HYDROQUINONE 
Recover Lightening Complex with 4% hydroquinone lotion
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:71393-004
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HYDROQUINONE (HYDROQUINONE) HYDROQUINONE 0.04 g  in 1 g
Inactive Ingredients
Ingredient Name Strength
SODIUM METABISULFITE  
SODIUM PALMITOYL PROLINE  
POTASSIUM SORBATE  
TROLAMINE  
NYMPHAEA ALBA FLOWER  
GLYCOLIC ACID  
.ALPHA.-BISABOLOL, (+/-)-  
ZINGIBER OFFICINALE WHOLE  
PHENOXYETHANOL  
CAPRYLYL GLYCOL  
UNDECYLENOYL PHENYLALANINE  
ALCOHOL  
C13-14 ISOPARAFFIN  
LAURETH-7  
GLYCERIN  
BUTYLENE GLYCOL  
PENTYLENE GLYCOL  
HYDROXYPHENYL PROPAMIDOBENZOIC ACID  
POLYACRYLAMIDE (10000 MW)  
HEXYLENE GLYCOL  
WATER  
SODIUM POLYACRYLATE (2500000 MW)  
PPG-3 BENZYL ETHER MYRISTATE  
DIMETHYLMETHOXY CHROMANYL PALMITATE  
DISODIUM HEDTA  
LOW DENSITY POLYETHYLENE  
Packaging
# Item Code Package Description
1 NDC:71393-004-50 50 g in 1 BOTTLE, PUMP
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 02/16/2011
Labeler - The Skin Atelier, Inc. (135049810)
Establishment
Name Address ID/FEI Operations
The Skin Atelier, Inc. 135049810 manufacture(71393-004)
Revised: 05/2017
 
The Skin Atelier, Inc.



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