IVERMECTIN 1% / METRONIDAZOLE 1%- ivermectin 1% / metronidazole 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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IVERMECTIN 1% / METRONIDAZOLE 1%

Directions for use

x

Sincerus Florida, LLC adverse reactions.

p

Active, Inactive

h

NDC 72934-1130-2 IVERMECTIN USP 1% / METRONIDAZOLE USP 1% gel 30 gm

c

IVERMECTIN 1% / METRONIDAZOLE 1% 
ivermectin 1% / metronidazole 1% gel
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:72934-1130
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
METRONIDAZOLE (UNII: 140QMO216E) (METRONIDAZOLE - UNII:140QMO216E) METRONIDAZOLE1 g  in 100 g
IVERMECTIN (UNII: 8883YP2R6D) (IVERMECTIN - UNII:8883YP2R6D) IVERMECTIN1 g  in 100 g
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72934-1130-230 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(72934-1130)

Revised: 4/2019
Document Id: 874c79d7-7767-3d66-e053-2995a90a6d5c
Set id: 874c79d7-7766-3d66-e053-2995a90a6d5c
Version: 1
Effective Time: 20190424
 
Sincerus Florida, LLC