KDMAN

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: KDMAN
Generic name: TOLNAFTATE
Manufacturer: Dongguan Youmi Trading Co., Ltd
Product type: HUMAN OTC DRUG
SPL set ID: 52a4e836-2059-a49f-e063-6394a90a6556
SPL ID: 52a4e836-205a-a49f-e063-6394a90a6556
Version: 1
Effective date: 2026-05-25
Source export date: 2026-10-12
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:46:11

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		KDMAN	openfda.brand_name
generic name		TOLNAFTATE	openfda.generic_name
manufacturer name		Dongguan Youmi Trading Co., Ltd	openfda.manufacturer_name
ndc	package	87723-6625-1	openfda.package_ndc
ndc	product	87723-6625	openfda.product_ndc
ndc11	package	87723662501	derived:openfda.package_ndc
rxcui		2689792	openfda.rxcui
spl id		52a4e836-205a-a49f-e063-6394a90a6556	id
spl set id		52a4e836-2059-a49f-e063-6394a90a6556	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 eyes. Stop use and ask a doctor if Irritation occurs. There is no improvement within 4 weeks for athlete's foot or ringworm, or 2 weeks for jock itch.

Reported adverse events (FAERS/openFDA)#

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