Dynarex 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: Dynarex Antifungal
Generic name: ANTIFUNGAL
Manufacturer: Dynarex Corporation
Product type: HUMAN OTC DRUG
SPL set ID: ab5b6467-c158-4407-9d52-3c0731030680
SPL ID: 2758be66-4129-317b-e063-6394a90a712a
Version: 9
Effective date: 2024-11-20
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:53:40

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 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M005	openfda.application_number
brand name		Dynarex Antifungal	openfda.brand_name
generic name		ANTIFUNGAL	openfda.generic_name
manufacturer name		Dynarex Corporation	openfda.manufacturer_name
ndc	package	67777-231-11	openfda.package_ndc
ndc	package	67777-231-12	openfda.package_ndc
ndc	package	67777-231-10	openfda.package_ndc
ndc	package	67777-231-02	openfda.package_ndc
ndc	package	67777-231-13	openfda.package_ndc
ndc	package	67777-231-01	openfda.package_ndc
ndc	product	67777-231	openfda.product_ndc
ndc11	package	67777023110	derived:openfda.package_ndc
ndc11	package	67777023102	derived:openfda.package_ndc
ndc11	package	67777023113	derived:openfda.package_ndc
ndc11	package	67777023101	derived:openfda.package_ndc
ndc11	package	67777023111	derived:openfda.package_ndc
ndc11	package	67777023112	derived:openfda.package_ndc
rxcui		309367	openfda.rxcui
spl id		2758be66-4129-317b-e063-6394a90a712a	id
spl set id		ab5b6467-c158-4407-9d52-3c0731030680	set_id
unii		G07GZ97H65	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 Do not use: Do not use on children under 2 years of age unless directed by a doctor. Avoid contact with eyes. For athletes foot and ringworm - if irritation occurs, or if there is no improvement within 4 weeks, discontinue use and consult a doctor. For jock itch - if irritation occurs, or if there is no improvement within two weeks, discontinue use and consult 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.