Private Label Antifungal Barrier Cream

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: Private Label Antifungal Barrier Cream
Generic name: 2% MICONAZOLE NITRATE CREAM
Manufacturer: Swiss-American CDMO, LLC
Product type: HUMAN OTC DRUG
SPL set ID: e74bddea-c1ac-4e4e-84bd-5a9defb85b2d
SPL ID: e08800a5-05ac-44be-8dc0-33ecb00aac38
Version: 4
Effective date: 2026-01-08
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 05:46:48

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Private Label Antifungal Barrier Cream	openfda.brand_name
generic name		2% MICONAZOLE NITRATE CREAM	openfda.generic_name
manufacturer name		Swiss-American CDMO, LLC	openfda.manufacturer_name
ndc	package	60232-0009-5	openfda.package_ndc
ndc	package	60232-0009-2	openfda.package_ndc
ndc	package	60232-0009-4	openfda.package_ndc
ndc	product	60232-0009	openfda.product_ndc
ndc11	package	60232000902	derived:openfda.package_ndc
ndc11	package	60232000904	derived:openfda.package_ndc
ndc11	package	60232000905	derived:openfda.package_ndc
rxcui		998483	openfda.rxcui
spl id		e08800a5-05ac-44be-8dc0-33ecb00aac38	id
spl set id		e74bddea-c1ac-4e4e-84bd-5a9defb85b2d	set_id
unii		VW4H1CYW1K	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. Not intended for ingestion. Do not use on children under 2 years of age unless directed by a doctor. Avoid contact with the eyes. For the treatment of athlete’s foot and ringworm: if irritation occurs or if there is no improvement within 4 weeks, discontinue use and consult a doctor. For the treatment of jock itch: if irritation occurs or there is no improvement within 2 weeks discontinue use and consult a doctor. Do not use for diaper rash. Keep out of the reach of children. If product is 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.