Natural Vine Fungal Nail patches

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: Natural Vine Fungal Nail patches
Generic name: TOLNAFTATE 1%
Manufacturer: GETHSEMANE BRANCH CORPORATION
Product type: HUMAN OTC DRUG
SPL set ID: 57905962-0745-ceee-e063-6294a90a88dd
SPL ID: 57905962-0746-ceee-e063-6294a90a88dd
Version: 1
Effective date: 2026-07-26
Source export date: 2026-09-28
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/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:48:27

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		Natural Vine Fungal Nail patches	openfda.brand_name
generic name		TOLNAFTATE 1%	openfda.generic_name
manufacturer name		GETHSEMANE BRANCH CORPORATION	openfda.manufacturer_name
ndc	package	87870-005-01	openfda.package_ndc
ndc	product	87870-005	openfda.product_ndc
ndc11	package	87870000501	derived:openfda.package_ndc
rxcui		2677690	openfda.rxcui
spl id		57905962-0746-ceee-e063-6294a90a88dd	id
spl set id		57905962-0745-ceee-e063-6294a90a88dd	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 on children under 2 years of age unless directed by a doctor on diaper rash Avoid contact with eyes, do not exceed the recommended daily dosage unless directed by a doctor. irritation occurs. there is no improvement within 4 weeks. ask a health professional before use. In case of a ccidental ingestion, seek medical advice immediately or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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