Lasolex AL

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: Lasolex AL
Generic name: MICONAZOLE NITRATE 2% ANTIFUNGAL
Manufacturer: PureTek Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 534df9be-b47a-03a1-e063-6394a90a265a
SPL ID: 534df9be-b47b-03a1-e063-6394a90a265a
Version: 1
Effective date: 2026-06-02
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/2026-11-06/90742968499056f8845d54427ea2950526b02c3f289aedd40679ed8e120a0e89/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run: 20261106T075659Z
Imported at: 2026-11-06 08:43:39

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		Lasolex AL	openfda.brand_name
generic name		MICONAZOLE NITRATE 2% ANTIFUNGAL	openfda.generic_name
manufacturer name		PureTek Corporation	openfda.manufacturer_name
ndc	package	59088-238-03	openfda.package_ndc
ndc	product	59088-238	openfda.product_ndc
ndc11	package	59088023803	derived:openfda.package_ndc
rxcui		998525	openfda.rxcui
rxcui		2746503	openfda.rxcui
spl id		534df9be-b47b-03a1-e063-6394a90a265a	id
spl set id		534df9be-b47a-03a1-e063-6394a90a265a	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 use 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.