METRONIDAZOLE 1% / MUPIROCIN 2% ointment

METRONIDAZOLE 1% / MUPIROCIN 2% by

Drug Labeling and Warnings

METRONIDAZOLE 1% / MUPIROCIN 2% by is a Prescription medication manufactured, distributed, or labeled by Sincerus Florida, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Directions for use

Sincerus Florida, LLC. Adverse reactions

Active, inactive

NDC 72934- 5143-2 METRONIDAZOLE USP 1% / MUPIROCIN USP 2%. Ointment 30gm

INGREDIENTS AND APPEARANCE

METRONIDAZOLE 1% / MUPIROCIN 2% 
metronidazole 1% / mupirocin 2% ointment

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 72934-5143
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
METRONIDAZOLE (UNII: 140QMO216E) (METRONIDAZOLE - UNII:140QMO216E)	METRONIDAZOLE	1 g  in 100 g
MUPIROCIN (UNII: D0GX863OA5) (MUPIROCIN - UNII:D0GX863OA5)	MUPIROCIN	2 g  in 100 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72934-5143-2	30 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/15/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/15/2019

Labeler - Sincerus Florida, LLC (080105003)

Establishment
Name	Address	ID/FEI	Business Operations
Sincerus Florida, LLC		080105003	manufacture(72934-5143)