HYDROCORTISONE 0.5% / HYDROQUINONE 6%- hydrocortisone 0.5% / 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.

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HYDROCORTISONE 0.5% / HYDROQUINONE 6%

Directions for use

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Sincerus Florida, LLC. Adverse reactions

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Active, inactive

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NDC 72934- 6103-2 HYDROCORTISONE USP 0.5% / HYDROQUINONE USP 6%. Emulsion 30 gm

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HYDROCORTISONE 0.5% / HYDROQUINONE 6% 
hydrocortisone 0.5% / hydroquinone 6% emulsion
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:72934-6103
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE0.5 g  in 100 g
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:72934-6103-230 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/17/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/17/2019
Labeler - Sincerus Florida, LLC (080105003)
Establishment
NameAddressID/FEIBusiness Operations
Sincerus Florida, LLC080105003manufacture(72934-6103)

Revised: 5/2019
Document Id: 891b8093-b045-7da5-e053-2a95a90ae31b
Set id: 891b8093-b044-7da5-e053-2a95a90ae31b
Version: 1
Effective Time: 20190517
 
Sincerus Florida, LLC