Package 83004-016-01

Brand: antifungal foot treatment

Generic: butenafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 83004-016-01
Digits Only 8300401601
Product NDC 83004-016
Product ID 83004-016_2fae9415-875b-58bc-e063-6394a90a3612
Description

1 TUBE in 1 CARTON (83004-016-01) / 20 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2025-02-27
Brand antifungal foot treatment
Generic butenafine hydrochloride
Sample Package No

Linked Drug Pages (1)

Antifungal Foot Treatment ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "2fae9415-875b-58bc-e063-6394a90a3612", "openfda": {"unii": ["R8XA2029ZI"], "spl_set_id": ["3a735ca5-4717-43a1-ab42-76f310bcfe00"], "manufacturer_name": ["Rida LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (83004-016-01)  / 20 g in 1 TUBE", "package_ndc": "83004-016-01", "marketing_start_date": "20250227"}], "brand_name": "Antifungal Foot Treatment", "product_id": "83004-016_2fae9415-875b-58bc-e063-6394a90a3612", "dosage_form": "GEL", "pharm_class": ["Benzylamine Antifungal [EPC]", "Benzylamines [CS]"], "product_ndc": "83004-016", "generic_name": "Butenafine Hydrochloride", "labeler_name": "Rida LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Antifungal Foot Treatment", "active_ingredients": [{"name": "BUTENAFINE HYDROCHLORIDE", "strength": "10 mg/g"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20250227", "listing_expiration_date": "20261231"}