Dermatool Fungal Nail Treatment

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: Dermatool Fungal Nail Treatment
Generic name: TOLNAFTATE 1%
Manufacturer: Papalo Group LLC
Product type: HUMAN OTC DRUG
SPL set ID: 2d2c0e12-123d-75bd-e063-6394a90ae546
SPL ID: 2d2c0e12-123e-75bd-e063-6394a90ae546
Version: 1
Effective date: 2025-01-31
Source export date: 2026-11-06
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/824fe785252d7061429a95ddb6de517ee399ef628d34e8fdcc3591ded286ae33/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:24:31

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		Dermatool Fungal Nail Treatment	openfda.brand_name
generic name		TOLNAFTATE 1%	openfda.generic_name
manufacturer name		Papalo Group LLC	openfda.manufacturer_name
ndc	package	84728-510-03	openfda.package_ndc
ndc	package	84728-510-02	openfda.package_ndc
ndc	package	84728-510-01	openfda.package_ndc
ndc	product	84728-510	openfda.product_ndc
ndc11	package	84728051001	derived:openfda.package_ndc
ndc11	package	84728051002	derived:openfda.package_ndc
ndc11	package	84728051003	derived:openfda.package_ndc
rxcui		313423	openfda.rxcui
spl id		2d2c0e12-123e-75bd-e063-6394a90ae546	id
spl set id		2d2c0e12-123d-75bd-e063-6394a90ae546	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

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 and ringworm).

Reported adverse events (FAERS/openFDA)#

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