Maximum Strength Antifungal Liquid

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: Maximum Strength Antifungal Liquid
Generic name: TOLNAFTATE
Manufacturer: WinCo Foods LLC
Product type: HUMAN OTC DRUG
SPL set ID: 15d9c11d-59cf-d1ed-e063-6394a90a90b6
SPL ID: 3810f05e-7fc2-bdab-e063-6294a90abba7
Version: 2
Effective date: 2025-06-21
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:25:11

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M005	openfda.application_number
brand name		Maximum Strength Antifungal Liquid	openfda.brand_name
generic name		TOLNAFTATE	openfda.generic_name
manufacturer name		WinCo Foods LLC	openfda.manufacturer_name
ndc	package	67091-753-30	openfda.package_ndc
ndc	product	67091-753	openfda.product_ndc
ndc11	package	67091075330	derived:openfda.package_ndc
rxcui		313423	openfda.rxcui
spl id		3810f05e-7fc2-bdab-e063-6294a90abba7	id
spl set id		15d9c11d-59cf-d1ed-e063-6394a90a90b6	set_id
unii		06KB629TKV	openfda.unii

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

Warnings For external use only. Do not use on children under 2 years of age unless directed by a doctor. When using this product avoid contact with the eyes. Stop use and consult a doctor if irritation occurs there is no improvement within 4 weeks Keep out of reach of children. If accidental ingestion occurs, 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.