Athlete Foot Treatment Kit

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Athlete Foot Treatment Kit
Generic name: TERBINAFINE HYDROCHLORIDE, TOLNAFTATE
Manufacturer: Beautivity LLC
Product type: HUMAN OTC DRUG
SPL set ID: 3b3aa69f-4e73-cabc-e063-6294a90ab65b
SPL ID: 5566fc4d-92a2-8e17-e063-6394a90aabe6
Version: 3
Effective date: 2026-06-29
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:15:17

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M005	openfda.application_number
brand name		Athlete Foot Treatment Kit	openfda.brand_name
generic name		TERBINAFINE HYDROCHLORIDE, TOLNAFTATE	openfda.generic_name
manufacturer name		Beautivity LLC	openfda.manufacturer_name
ndc	package	85398-008-01	openfda.package_ndc
ndc	package	85398-007-01	openfda.package_ndc
ndc	package	85398-006-01	openfda.package_ndc
ndc	product	85398-008	openfda.product_ndc
ndc11	package	85398000801	derived:openfda.package_ndc
ndc11	package	85398000701	derived:openfda.package_ndc
ndc11	package	85398000601	derived:openfda.package_ndc
rxcui		1807715	openfda.rxcui
rxcui		992528	openfda.rxcui
spl id		5566fc4d-92a2-8e17-e063-6394a90aabe6	id
spl set id		3b3aa69f-4e73-cabc-e063-6294a90ab65b	set_id

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

For external use only on children under 2 years of age unless directed by a doctor on nails and scalp in or near the mouth or eyes for vaginal yeast infections When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water. Stop use and ask a doctor If irritatioin occurs or there is no improvement within 2 weeks. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.