NDC 72934-1237

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

171083 Ivermectin 1% / Metronidazole 1% / Niacinamide 4%

171083 IVERMECTIN 1% / METRONIDAZOLE 1% / NIACINAMIDE 4% is a Topical Gel in the Human Prescription Drug category. It is labeled and distributed by Sincerus Florida, Llc. The primary component is Metronidazole; Niacinamide; Ivermectin.

Product ID72934-1237_a97b3663-5150-2f2f-e053-2a95a90ad69a
NDC72934-1237
Product TypeHuman Prescription Drug
Proprietary Name171083 IVERMECTIN 1% / METRONIDAZOLE 1% / NIACINAMIDE 4%
Generic Name171083 Ivermectin 1% / Metronidazole 1% / Niacinamide 4%
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2020-07-02
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameSincerus Florida, LLC
Substance NameMETRONIDAZOLE; NIACINAMIDE; IVERMECTIN
Active Ingredient Strength1 g/100g; g/100g; g/100g
Pharm ClassesNitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS],Antiparasitic [EPC],Pediculicide [EPC]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 72934-1237-2

30 g in 1 BOTTLE, PUMP (72934-1237-2)
Marketing Start Date2020-07-02
NDC Exclude FlagN
Sample Package?N

Drug Details


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