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: Antifungal
Generic name: CLOTRIMAZOLE
Manufacturer: Dynarex Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 4d4cc4b4-c0b4-9e25-e063-6294a90a70b8
SPL ID: 4d4cc4b4-c0b5-9e25-e063-6294a90a70b8
Version: 1
Effective date: 2026-03-18
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:26:05

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 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M005	openfda.application_number
brand name		Antifungal	openfda.brand_name
generic name		CLOTRIMAZOLE	openfda.generic_name
manufacturer name		Dynarex Corporation	openfda.manufacturer_name
ndc	package	67777-727-02	openfda.package_ndc
ndc	package	67777-727-04	openfda.package_ndc
ndc	package	67777-727-05	openfda.package_ndc
ndc	package	67777-727-03	openfda.package_ndc
ndc	package	67777-727-01	openfda.package_ndc
ndc	product	67777-727	openfda.product_ndc
ndc11	package	67777072701	derived:openfda.package_ndc
ndc11	package	67777072702	derived:openfda.package_ndc
ndc11	package	67777072703	derived:openfda.package_ndc
ndc11	package	67777072705	derived:openfda.package_ndc
ndc11	package	67777072704	derived:openfda.package_ndc
rxcui		309367	openfda.rxcui
spl id		4d4cc4b4-c0b5-9e25-e063-6294a90a70b8	id
spl set id		4d4cc4b4-c0b4-9e25-e063-6294a90a70b8	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 on children under 2 years of age unless directed by a doctor • For external use only • Avoid contact with eyes Stop use and ask a doctor if • Irritation occurs or if there is no improvement within 4 weeks, discontinue use and consult a doctor for athlete's foot and ringworm. • Irritation occurs or if there is no improvement within 2 weeks, discontinue use and consult a doctor for jock itch. Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away

Reported adverse events (FAERS/openFDA)#

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