Zeasorb Jock Itch

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: Zeasorb Jock Itch
Generic name: MICONAZOLE NITRATE
Manufacturer: Crown Laboratories
Product type: HUMAN OTC DRUG
SPL set ID: 09d088ef-aab3-5565-e063-6394a90af263
SPL ID: 4833f63f-c8ac-19bf-e063-6394a90abcdc
Version: 3
Effective date: 2026-01-12
Source export date: 2026-10-30
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/2026-10-30/0b630a6825fc0c8abba22d7c8fd4d069bde78bef928766047ddbb369119f337f/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:59:03

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M005	openfda.application_number
brand name		Zeasorb Jock Itch	openfda.brand_name
generic name		MICONAZOLE NITRATE	openfda.generic_name
manufacturer name		Crown Laboratories	openfda.manufacturer_name
ndc	package	0316-8001-02	openfda.package_ndc
ndc	product	0316-8001	openfda.product_ndc
ndc11	package	00316800102	derived:openfda.package_ndc
rxcui		1437793	openfda.rxcui
rxcui		998461	openfda.rxcui
spl id		4833f63f-c8ac-19bf-e063-6394a90abcdc	id
spl set id		09d088ef-aab3-5565-e063-6394a90af263	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. Avoid contact with the eyes. Do not use on children under 2 years of age unless directed by a doctor. If irritation occurs or if there is no improvement within 2 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.