LEVOCETIRIZINE DIHYDROCHLORIDE 2% / MUPIROCIN 2% / TRIAMCINOLONE ACETONIDE 0.025%- levocetirizine dihydrochloride 2% / mupirocin 2% / triamcinolone acetonide 0.025% cream 
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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LEVOCETIRIZINE DIHYDROCHLORIDE 2% / MUPIROCIN 2% / TRIAMCINOLONE ACETONIDE 0.025%

Directions for use

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Sincerus Florida, LLC. Adverse reactions

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Active, inactive

 x

NDC 72934- 2137-2 LEVOCETIRIZINE DIHYDROCHLORIDE USP 2% / MUPIROCIN USP 2% / TRIAMCINOLONE ACETONIDE USP 0.025%. Cream 30gm

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LEVOCETIRIZINE DIHYDROCHLORIDE 2% / MUPIROCIN 2% / TRIAMCINOLONE ACETONIDE 0.025% 
levocetirizine dihydrochloride 2% / mupirocin 2% / triamcinolone acetonide 0.025% cream
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:72934-2137
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LEVOCETIRIZINE DIHYDROCHLORIDE (UNII: SOD6A38AGA) (LEVOCETIRIZINE - UNII:6U5EA9RT2O) LEVOCETIRIZINE DIHYDROCHLORIDE2 g  in 100 g
MUPIROCIN (UNII: D0GX863OA5) (MUPIROCIN - UNII:D0GX863OA5) MUPIROCIN2 g  in 100 g
TRIAMCINOLONE ACETONIDE (UNII: F446C597KA) (TRIAMCINOLONE ACETONIDE - UNII:F446C597KA) TRIAMCINOLONE ACETONIDE0.025 g  in 100 g
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72934-2137-230 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(72934-2137)

Revised: 5/2019
Document Id: 88debe23-e0a1-1236-e053-2a95a90ac9a6
Set id: 88debe23-e0a0-1236-e053-2a95a90ac9a6
Version: 1
Effective Time: 20190514
 
Sincerus Florida, LLC