Home NDC 70677-1269 Athletes Foot
Product NDC 70677-1269
11-digit product format 706771269
Labeler code 70677
Product ID 70677-1269_3906735f-2b7e-1157-e063-6394a90a61e3
Type HUMAN OTC DRUG
Nonproprietary name BUTENAFINE HYDROCHLORIDE
Dosage form CREAM
Route TOPICAL
Labeler STRATEGIC SOURCING SERVICES LLC
Application ANDA205181
Marketing category ANDA
Marketing start 2024-11-07
Substance BUTENAFINE HYDROCHLORIDE
Active strength 10 mg/g
Pharmacologic classes Benzylamine Antifungal [EPC], Benzylamines [CS]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Source provenance: Browse the complete Orange Book source catalog · source snapshot 1 .
Orange Book products# Current product rows page 1 of 1 · 1 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A205181-001 BUTENAFINE HYDROCHLORIDE BUTENAFINE HYDROCHLORIDE 1% CREAM / TOPICAL 2017-11-16
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-08-01 22:54:32 2026-06 A205181-001 BUTENAFINE HYDROCHLORIDE 1% CREAM / TOPICAL 2017-11-16 a50c72e98297…
openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
Matched openFDA labels page 1 of 1 · 18 matching rows.
Additional Listing Data#
Finished product Yes
Brand name base Athletes Foot
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BUTENAFINE HYDROCHLORIDE 10 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination R8XA2029ZI Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1298448 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70677-1269-1 Athletes Foot 30 g in 1 TUBE CREAM 30 3 70677-1269-1 Athletes Foot 1 in 1 CARTON CREAM 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70677-1269 ATHLETES FOOT (BUTENAFINE HYDROCHLORIDE) CREAM [STRATEGIC SOURCING SERVICES LLC] 2 Current NDC, 2 package rows 20241116_b4913a89-56fd-4710-b28e-6fb6d50fd3f3.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 70677-1269-1 70677126901 1 TUBE in 1 CARTON (70677-1269-1) / 30 g in 1 TUBE 1 tube 2024-11-07 No No Current