141055 HYDROQUINONE 6%- 141055 hydroquinone 6% 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.

----------

141055 HYDROQUINONE 6%

Directions for use

fd

Sincerus Florida, LLC adverse reactions

jg

Active Inactive

s

NDC 72934-6230-2 141055 HYDROQUINONE 6% Emulsion 30 gm

5

141055 HYDROQUINONE 6% 
141055 hydroquinone 6% emulsion
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:72934-6230
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE) HYDROQUINONE6 g  in 100 g
Product Characteristics
Coloryellow (Beige) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72934-6230-230 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product07/02/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other07/02/2020
Labeler - Sincerus Florida, LLC (080105003)
Establishment
NameAddressID/FEIBusiness Operations
Sincerus Florida, LLC080105003manufacture(72934-6230)

Revised: 7/2020
Document Id: a979ee53-dea4-0bc9-e053-2a95a90ac8b0
Set id: a979ee53-dea3-0bc9-e053-2a95a90ac8b0
Version: 1
Effective Time: 20200702
 
Sincerus Florida, LLC