HYDROQUINONE 8%- hydroquinone 8% emulsion 
Sincerus Florida, LLC

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.

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HYDROQUINONE 8%

Directions for use

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Sincerus Florida, LLC adverse reactions.

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Active, inactive

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NDC 72934-6121-2 Hydroquinone USP 8%.
Emulsion 30gm

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HYDROQUINONE 8% 
hydroquinone 8% emulsion
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:72934-6121
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE) HYDROQUINONE8 g  in 100 g
Product Characteristics
Coloryellow (BEIGE OPAQUE) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72934-6121-230 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/01/2019
Labeler - Sincerus Florida, LLC (080105003)
Establishment
NameAddressID/FEIBusiness Operations
Sincerus Florida, LLC080105003manufacture(72934-6121)

Revised: 4/2019
Document Id: 874c1900-82ed-4082-e053-2995a90aff22
Set id: 874c1900-82ec-4082-e053-2995a90aff22
Version: 1
Effective Time: 20190424
 
Sincerus Florida, LLC