51672-2101 : Jock Itch 10 mg/g Topical Cream


NDC: 51672-2101
Labeler: Taro Pharmaceuticals U.S.a., Inc.
Product Type: Human OTC Drug
Drug Name:  Jock Itch
Dosage Form: Topical Cream
Application #: ANDA205181
Rev. Date: 


NDC Package Codes:

  • 51672-2101-1: 1 TUBE IN 1 CARTON (51672‑2101‑1) > 15 G IN 1 TUBE
  • 51672-2101-2: 1 TUBE IN 1 CARTON (51672‑2101‑2) > 30 G IN 1 TUBE
  • 51672-2101-8: 1 TUBE IN 1 CARTON (51672‑2101‑8) > 12 G IN 1 TUBE
  • 51672-2101-9: 1 TUBE IN 1 CARTON (51672‑2101‑9) > 24 G IN 1 TUBE

Active Ingredients:

  • Butenafine Hydrochloride

Dosage Strength:

  • 10 mg/g

Related Products:

Based on records with the same trade name.
  • 0363-0695 Jock Itch 1 g/100g Topical Spray by Walgreen Company
  • 0363-1497 Jock Itch 2 g/100g Topical Spray by Walgreen Company
  • 0363-2101 Jock Itch 10 mg/g Topical Cream by Walgreen Company
  • 0363-3510 Jock Itch 1 g/100g Topical Cream by Walgreen Company
  • 11673-062 Jock Itch 10 mg/g Topical Cream by Target Corporation
  • 11822-0504 Jock Itch 1 g/100g Topical Cream by Rite Aid Corporation
  • 11822-0695 Jock Itch 1 g/100g Topical Spray by Rite Aid Corporation
  • 72103-525 Jock Itch 1 g/100g Topical Cream by The Ibn Sina Pharmaceutical Industry Ltd.
  • 79481-0602 Jock Itch 20 mg/g Topical Aerosol, Spray by Meijer Distribution Inc.

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.