PENTOXIFYLLINE 0.5% / TRIAMCINOLONE ACETONIDE 0.1%- pentoxifylline 0.5% / triamcinolone acetonide 0.1% 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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PENTOXIFYLLINE 0.5% / TRIAMCINOLONE ACETONIDE 0.1%

Directions for use

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Sincerus Florida, LLC. Adverse reactions

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Active, inactive

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NDC 72934- 1169-2 PENTOXIFYLLINE USP 0.5% / TRIAMCINOLONE ACETONIDE USP 0.1%. Gel 30gm.

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PENTOXIFYLLINE 0.5% / TRIAMCINOLONE ACETONIDE 0.1% 
pentoxifylline 0.5% / triamcinolone acetonide 0.1% gel
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:72934-1169
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PENTOXIFYLLINE (UNII: SD6QCT3TSU) (PENTOXIFYLLINE - UNII:SD6QCT3TSU) PENTOXIFYLLINE0.5 g  in 100 g
TRIAMCINOLONE ACETONIDE (UNII: F446C597KA) (TRIAMCINOLONE ACETONIDE - UNII:F446C597KA) TRIAMCINOLONE ACETONIDE0.1 g  in 100 g
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72934-1169-230 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/15/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/15/2019
Labeler - Sincerus Florida, LLC (080105003)
Establishment
NameAddressID/FEIBusiness Operations
Sincerus Florida, LLC080105003manufacture(72934-1169)

Revised: 5/2019
Document Id: 88dee26d-be0a-5ae2-e053-2995a90ac52c
Set id: 88dee26d-be09-5ae2-e053-2995a90ac52c
Version: 1
Effective Time: 20190514
 
Sincerus Florida, LLC