NDC 72934-1130

IVERMECTIN 1% / METRONIDAZOLE 1%

Ivermectin 1% / Metronidazole 1%

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

Product ID72934-1130_874c79d7-7767-3d66-e053-2995a90a6d5c
NDC72934-1130
Product TypeHuman Prescription Drug
Proprietary NameIVERMECTIN 1% / METRONIDAZOLE 1%
Generic NameIvermectin 1% / Metronidazole 1%
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2019-05-01
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameSincerus Florida, LLC
Substance NameMETRONIDAZOLE; IVERMECTIN
Active Ingredient Strength1 g/100g; g/100g
Pharm ClassesNitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS],Antiparasitic [EPC],Pediculicide [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 72934-1130-2

30 g in 1 BOTTLE, PUMP (72934-1130-2)
Marketing Start Date2019-05-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 72934-1130-2 [72934113002]

IVERMECTIN 1% / METRONIDAZOLE 1% GEL
Marketing Categoryunapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-05-01

Drug Details

Active Ingredients

IngredientStrength
METRONIDAZOLE1 g/100g

Pharmacological Class

  • Nitroimidazole Antimicrobial [EPC]
  • Nitroimidazoles [CS]
  • Antiparasitic [EPC]
  • Pediculicide [EPC]
  • Nitroimidazole Antimicrobial [EPC]
  • Nitroimidazoles [CS]
  • Antiparasitic [EPC]
  • Pediculicide [EPC]
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