FUNGINIX AF

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: FUNGINIX AF
Generic name: TOLNAFTATE
Manufacturer: The Sisquoc Healthcare Corporation
Product type: HUMAN OTC DRUG
SPL set ID: f6cf5315-6678-486c-85b2-d4b3f748600e
SPL ID: 2f007d49-0eeb-511e-e063-6394a90ae3f8
Version: 7
Effective date: 2025-02-25
Source export date: 2026-09-28
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:37:08

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		FUNGINIX AF	openfda.brand_name
generic name		TOLNAFTATE	openfda.generic_name
manufacturer name		The Sisquoc Healthcare Corporation	openfda.manufacturer_name
ndc	package	71229-103-11	openfda.package_ndc
ndc	product	71229-103	openfda.product_ndc
ndc11	package	71229010311	derived:openfda.package_ndc
rxcui		103951	openfda.rxcui
spl id		2f007d49-0eeb-511e-e063-6394a90ae3f8	id
spl set id		f6cf5315-6678-486c-85b2-d4b3f748600e	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. IF CONTACT OCCURS, RINSE THE EYES VERY THOROUGHLY WITH WATER. STOP USE AND ASK A DOCTOR IF IRRITATION OCCURS OR THERE IS NO IMPROVEMENT WITHIN 4 WEEKS.

Reported adverse events (FAERS/openFDA)#

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