NIACINAMIDE 4% / TRETINOIN 0.05%- niacinamide 4% / tretinoin 0.05% gel 
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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NIACINAMIDE 4% / TRETINOIN 0.05%

Directions for use

f

Sincerus Florida, LLC adverse reactions.

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Active, Inactive

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NDC 72934-1163-2
Niacinamide USP 4% Tretinoin USP 0.05 %
Gel 30gm

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NIACINAMIDE 4% / TRETINOIN 0.05% 
niacinamide 4% / tretinoin 0.05% gel
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:72934-1163
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRETINOIN (UNII: 5688UTC01R) (TRETINOIN - UNII:5688UTC01R) TRETINOIN0.05 g  in 100 g
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE4 g  in 100 g
Product Characteristics
ColoryellowScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72934-1163-230 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(72934-1163)

Revised: 4/2019
Document Id: 8737e771-b3bf-1010-e053-2991aa0a9393
Set id: 8737e771-b3be-1010-e053-2991aa0a9393
Version: 1
Effective Time: 20190423
 
Sincerus Florida, LLC