171083 IVERMECTIN 1% / METRONIDAZOLE 1% / NIACINAMIDE 4%

171083 IVERMECTIN 1% / METRONIDAZOLE 1% / NIACINAMIDE 4%- metronidazole, niacinamide and ivermectin 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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Sincerus Florida, LLC adverse reactions

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NDC 72934-1237-2 171083 IVERMECTIN 1% / METRONIDAZOLE 1% / NIACINAMIDE 4% gel 30 gm

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171083 IVERMECTIN 1% / METRONIDAZOLE 1% / NIACINAMIDE 4%
171083 ivermectin 1% / metronidazole 1% / niacinamide 4% gel
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-1237
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
METRONIDAZOLE (METRONIDAZOLE) METRONIDAZOLE 1 g in 100 g
NIACINAMIDE (NIACINAMIDE) NIACINAMIDE 4 g in 100 g
IVERMECTIN (IVERMECTIN) IVERMECTIN 1 g in 100 g
Product Characteristics
Color yellow Score
Shape Size
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:72934-1237-2 30 g in 1 BOTTLE, PUMP None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 07/02/2020
Labeler — Sincerus Florida, LLC (080105003)
Establishment
Name Address ID/FEI Operations
Sincerus Florida, LLC 080105003 manufacture (72934-1237)

Revised: 07/2020 Sincerus Florida, LLC

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