antifungal foot treatment
Generic: butenafine hydrochloride
Labeler: rida llcDrug Facts
Product Profile
Brand Name
antifungal foot treatment
Generic Name
butenafine hydrochloride
Labeler
rida llc
Dosage Form
GEL
Routes
Active Ingredients
butenafine hydrochloride 10 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
83004-016
Product ID
83004-016_2fae9415-875b-58bc-e063-6394a90a3612
Product Type
HUMAN OTC DRUG
Marketing Category
UNAPPROVED HOMEOPATHIC
Listing Expiration
2026-12-31
Marketing Start
2025-02-27
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
83004016
Hyphenated Format
83004-016
Supplemental Identifiers
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
antifungal foot treatment (source: ndc)
Generic Name
butenafine hydrochloride (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/g
Packaging
- 1 TUBE in 1 CARTON (83004-016-01) / 20 g in 1 TUBE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
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"}