Miconazorb 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: Miconazorb AF
Generic name: MICONAZOLE NITRATE
Manufacturer: AmerisourceBergen Drug Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 13a20d21-42d5-fe56-e063-6394a90aaf57
SPL ID: 42642785-742d-6084-e063-6294a90abf74
Version: 4
Effective date: 2025-10-30
Source export date: 2026-10-12
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/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:12:28

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		Miconazorb AF	openfda.brand_name
generic name		MICONAZOLE NITRATE	openfda.generic_name
manufacturer name		AmerisourceBergen Drug Corporation	openfda.manufacturer_name
ndc	package	46122-789-29	openfda.package_ndc
ndc	product	46122-789	openfda.product_ndc
ndc11	package	46122078929	derived:openfda.package_ndc
rxcui		998461	openfda.rxcui
spl id		42642785-742d-6084-e063-6294a90abf74	id
spl set id		13a20d21-42d5-fe56-e063-6394a90aaf57	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. Do not use on children under 2 years of age unless directed by a doctor. When using this product avoid contact with the eyes Stop and ask a doctor if irritation occurs or there is no improvement within 4 weeks for athlete's foot and ringworm, or 2 weeks for jock itch. 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.