sunmark antifungal

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: sunmark antifungal
Generic name: TOLNAFTATE
Manufacturer: A-S Medication Solutions
Product type: HUMAN OTC DRUG
SPL set ID: 6f85fbb0-297c-4949-83f2-ed9a52172154
SPL ID: 3802e6c5-c6f6-4ed5-80c9-97e5b0a38a5d
Version: 9
Effective date: 2023-12-16
Source export date: 2026-11-06
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/2026-11-06/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:01:04

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		sunmark antifungal	openfda.brand_name
generic name		TOLNAFTATE	openfda.generic_name
manufacturer name		A-S Medication Solutions	openfda.manufacturer_name
ndc	package	50090-3358-0	openfda.package_ndc
ndc	product	50090-3358	openfda.product_ndc
ndc11	package	50090335800	derived:openfda.package_ndc
rxcui		103951	openfda.rxcui
spl id		3802e6c5-c6f6-4ed5-80c9-97e5b0a38a5d	id
spl set id		6f85fbb0-297c-4949-83f2-ed9a52172154	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 When using this product avoid contact with the eyes Stop use and ask a doctor if irritation occurs there is no improvement within 4 weeks (for athlete's foot or ringworm) or within 2 weeks (for jock itch) Do not use on children under 2 years of age except under the advice and supervision of a doctor. Keep out of reach of children. 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.