RoyceDerm Antifungal Bar

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: RoyceDerm Antifungal Bar
Generic name: CLOTRIMAZOLE
Manufacturer: RoyceDerm LLC
Product type: HUMAN OTC DRUG
SPL set ID: 3abdc4a8-58dd-5bd0-e063-6294a90a1bca
SPL ID: 4e5e3a3a-ab41-10ca-e063-6294a90ace0e
Version: 2
Effective date: 2026-03-31
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 07:25:50

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 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M005	openfda.application_number
brand name		RoyceDerm Antifungal Bar	openfda.brand_name
generic name		CLOTRIMAZOLE	openfda.generic_name
manufacturer name		RoyceDerm LLC	openfda.manufacturer_name
ndc	package	85424-005-02	openfda.package_ndc
ndc	package	85424-005-01	openfda.package_ndc
ndc	product	85424-005	openfda.product_ndc
ndc11	package	85424000502	derived:openfda.package_ndc
ndc11	package	85424000501	derived:openfda.package_ndc
rxcui		251267	openfda.rxcui
spl id		4e5e3a3a-ab41-10ca-e063-6294a90ace0e	id
spl set id		3abdc4a8-58dd-5bd0-e063-6294a90a1bca	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

For externaluse only. on children under two years of age unless directed by a doctor. avoid contact withthe eyes. irritation occurs-there is no improvement within 2 weeks for jock itch or within 4 weeks for athlete's foot and ringworm. lf swallowed,call poison control or seek medical help.

Reported adverse events (FAERS/openFDA)#

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