83004-016 : Antifungal Foot Treatment 10 mg/g Topical Gel


NDC: 83004-016
Labeler: Rida LLC
Product Type: Human OTC Drug
Drug Name:  Antifungal Foot Treatment
Dosage Form: Topical Gel
Rev. Date: 


NDC Package Codes:

  • 83004-016-01: 1 TUBE IN 1 CARTON (83004‑016‑01) / 20 G IN 1 TUBE

Active Ingredients:

  • Butenafine Hydrochloride

Dosage Strength:

  • 10 mg/g

Pharmaceutical Classes:

  • Benzylamine Antifungal [EPC]
  • Benzylamines [CS]

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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.