DESOXIMETASONE 0.05% / HYDROQUINONE 6% / TRETINOIN 0.05%- desoximetasone 0.05% / hydroquinone 6% / tretinoin 0.05% 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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DESOXIMETASONE 0.05% / HYDROQUINONE 6% / TRETINOIN 0.05%

Directions for use

as

Sincerus Florida, LLC. Adverse reaction

vb

Active, inactive

sdf

NDC 72934- 6067-2 DESOXIMETASONE USP 0.05% / HYDROQUINONE USP 6% / TRETINOIN USP 0.05%. Emulsion 30 gm

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DESOXIMETASONE 0.05% / HYDROQUINONE 6% / TRETINOIN 0.05% 
desoximetasone 0.05% / hydroquinone 6% / tretinoin 0.05% emulsion
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:72934-6067
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DESOXIMETASONE (UNII: 4E07GXB7AU) (DESOXIMETASONE - UNII:4E07GXB7AU) DESOXIMETASONE0.05 g  in 100 g
HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE) HYDROQUINONE6 g  in 100 g
TRETINOIN (UNII: 5688UTC01R) (TRETINOIN - UNII:5688UTC01R) TRETINOIN0.05 g  in 100 g
Product Characteristics
ColoryellowScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72934-6067-230 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/21/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/21/2019
Labeler - Sincerus Florida, LLC (080105003)
Establishment
NameAddressID/FEIBusiness Operations
Sincerus Florida, LLC080105003manufacture(72934-6067)

Revised: 5/2019
Document Id: 89585e3f-167f-dd3b-e053-2995a90ade55
Set id: 89585e3f-167e-dd3b-e053-2995a90ade55
Version: 1
Effective Time: 20190520
 
Sincerus Florida, LLC