Lasolex Liquid Solution

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 Liquid Solution
Generic name: CLOTRIMAZOLE 1%
Manufacturer: PureTek Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 4dc9e64d-8235-b218-e063-6394a90a0157
SPL ID: 4dc9e65a-242c-c059-e063-6394a90a9344
Version: 1
Effective date: 2026-03-24
Source export date: 2026-09-28
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:39:20

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 Liquid Solution	openfda.brand_name
generic name		CLOTRIMAZOLE 1%	openfda.generic_name
manufacturer name		PureTek Corporation	openfda.manufacturer_name
ndc	package	59088-251-03	openfda.package_ndc
ndc	product	59088-251	openfda.product_ndc
ndc11	package	59088025103	derived:openfda.package_ndc
rxcui		309370	openfda.rxcui
rxcui		2739324	openfda.rxcui
spl id		4dc9e65a-242c-c059-e063-6394a90a9344	id
spl set id		4dc9e64d-8235-b218-e063-6394a90a0157	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

Warnings For external use only. Do not use on children under 2 years of age When using this product • avoid contact with eyes Stop use and ask a doctor if • for athlete's foot and ringworm, if irritation occurs or if there is no improvement within 4 weeks, discontinue use and consult a licensed healthcare practitioner • for jock itch, if irritation occurs or if there is no improvement in 2 weeks, discontinue use and consult a licensed healthcare practitioner 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.