Lasolex AG

Product NDC: 59088-207
11-digit product format: 590880207
Labeler code: 59088
Product ID: 59088-207_474761d7-e86c-6f50-e063-6394a90a07b4
Type: HUMAN OTC DRUG
Nonproprietary name: MICONAZOLE NITRATE
Dosage form: GEL
Route: TOPICAL
Labeler: Puretek Corporation
Application: M005
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2025-12-03
Substance: MICONAZOLE NITRATE
Active strength: 2 g/100g
Pharmacologic classes: Azole Antifungal [EPC], Azoles [CS]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product: Yes
Brand name base: Lasolex AG
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MICONAZOLE NITRATE	2 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
VW4H1CYW1K	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
998437	Internal RxNorm lookup
2735135	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
4411142f-a8ec-c8c2-e063-6394a90aa25c	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
3a55f4fb-5aec-4c88-0ff7-4d608ad4866a	Product name	1	20140508
5b9a7965-36d2-8412-dcaf-f76a65411611	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
59088-207-07	Lasolex AG	85 g in 1 TUBE	GEL	85		5

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
59088-207-07	GM - Gram	59088-207	c0429a15-b9c9-4029-a7a7-e056c9fc6bbb	1	2026-01-08

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 22 of 49 · 973 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Signature Select Advanced Hand Sanitizer	ALCOHOL	Living Better Brands LLC	6d1cc25b-d612-4aae-bdb0-304758ef8f0f	2026-01-26	Warnings	Exact identifier application number: M005
clotrimazole	CLOTRIMAZOLE	Padagis Israel Pharmaceuticals Ltd	3dcd0158-ec51-4fa7-a26a-02c2926156c0	2026-01-22	Warnings	Exact identifier application number: M005
Puriya Antifungal Balm	ZINC UNDECYLENATE	IPC Republic, Inc.	96bf44bc-b5eb-4198-9056-02e51665a162	2026-01-22	Warnings	Exact identifier application number: M005
BZK Antiseptic	BENZALKONIUM CHLORIDE	Lights Medical Manufacture Co., Ltd.	698ed472-9204-46e3-95a4-d59e204628ac	2026-01-21	Warnings	Exact identifier application number: M005
LIGHTS Swabstick	BENZALKONIUM CHLORIDE	Lights Medical Manufacture Co., Ltd.	9346512e-53a1-420a-8b4d-bfbec32576a2	2026-01-21	Warnings	Exact identifier application number: M005
Lights Isopropyl Alcohol Prep Pads	ISOPROPYL ALCOHOL	Lights Medical Manufacture Co., Ltd.	4905a27c-6cf8-4b1a-a02c-4c81756e8c0a	2026-01-21	Warnings	Exact identifier application number: M005
Bee Venom Fungal Nail Treatment Liquid	BEE VENOM FUNGAL NAIL TREATMENT	Shenzhen Earth Surface Trading Co., Ltd.	48d164bc-dab6-6fe4-e063-6394a90a3fc4	2026-01-20	Warnings	Exact identifier application number: M005
Tolnaftate	MEIJER ATHLETES FOOT LIQUID SPRAY	Meijer Distribution Inc.	d9f7753f-aef9-86e2-e053-2995a90a2082	2026-01-20	Warnings	Exact identifier application number: M005
Tolnaftate	FOOT ODOR CONTROL POWDER SPRAY	Meijer Distribution Inc	b3ba676e-9377-4665-b99e-d4143df96b36	2026-01-20	Warnings	Exact identifier application number: M005
Tolnaftate	MEIJER ATHLETES FOOT LIQUID	Meijer Distribution Inc.	0399dfef-9ea6-6fe4-e063-6394a90aec43	2026-01-20	Warnings	Exact identifier application number: M005
TOENAIL FUNGUS TREATMENT MAXIMUM STRENGTH Liquid	TOLNAFTATE	Shenzhen Ctrip Technology Co., Ltd.	1fb03184-5f21-c82a-e063-6294a90a9fa4	2026-01-19	Warnings	Exact identifier application number: M005
Miconazole Nitrate	MICONAZOLE NITRATE	AvKARE	1a26534d-eeb8-8d17-e063-6294a90a70c7	2026-01-19	Warnings	Exact identifier application number: M005
Hermon Antifungal Soap. 4 packs	TOLNAFTATE 1%	Beautivity LLC	42c769de-f1e1-b3a1-e063-6394a90ab2a1	2026-01-18	Warnings	Exact identifier application number: M005
Hermon Antifungal Cleansing Bar	TOLNAFTATE 1%	Beautivity LLC	48b5d7b3-a134-ecdd-e063-6294a90a3213	2026-01-18	Warnings	Exact identifier application number: M005
ANTIFUNGAL TOENAIL FUNGUS PEN	UNDECYLENIC ACID	Yunqi Cosmetics (Shenzhen) Co., Ltd	48b5fbd9-bdf5-21ac-e063-6394a90aa6b6	2026-01-18	Warnings	Exact identifier application number: M005
Hermon Antifungal Soap.	TOLNAFTATE 1%	Beautivity LLC	41e37014-549c-e592-e063-6294a90ac6ab	2026-01-17	Warnings	Exact identifier application number: M005
Hermon Antifungal .soap.	TOLNAFTATE 1%	Beautivity LLC	482c338f-870f-f6d7-e063-6394a90a432c	2026-01-17	Warnings	Exact identifier application number: M005
MEOLY Fungal Nail Renewal	FUNGAL NAIL RENEWAL	Shenzhen Xinxin Yunhai Technology Co., Ltd.	487d2e22-6328-893f-e063-6394a90a9dff	2026-01-16	Warnings	Exact identifier application number: M005
Lotrimin Antifungal	MICONAZOLE NITRATE	Bayer HealthCare LLC.	cebd222c-074f-443c-bd37-612114b27bbd	2026-01-16	Warnings	Exact identifier application number: M005
Lotrimin Daily Prevention	TOLNAFTATE	Bayer HealthCare LLC.	9e8f9211-e85d-725a-e053-2995a90a09b3	2026-01-16	Warnings	Exact identifier application number: M005

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
VW4H1CYW1K	MICONAZOLE NITRATE	22832-87-7	MICONAZOLE NITRATE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
2735135	Lasolex 2 % Topical Gel	PSN	4411142f-a8ec-c8c2-e063-6394a90aa25c	5
998437	miconazole nitrate 2 % Topical Gel	PSN	4411142f-a8ec-c8c2-e063-6394a90aa25c	5
2735135	miconazole nitrate 0.02 MG/MG Topical Gel [Lasolex]	SBD	4411142f-a8ec-c8c2-e063-6394a90aa25c	5
998437	miconazole nitrate 0.02 MG/MG Topical Gel	SCD	4411142f-a8ec-c8c2-e063-6394a90aa25c	5
2735135	Lasolex 0.02 MG/MG Topical Gel	SY	4411142f-a8ec-c8c2-e063-6394a90aa25c	5
2735135	Lasolex 2 % Topical Gel	SY	4411142f-a8ec-c8c2-e063-6394a90aa25c	5
998437	miconazole nitrate 2 % Topical Gel	SY	4411142f-a8ec-c8c2-e063-6394a90aa25c	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
59088-207-07	59088020707	85 g in 1 TUBE (59088-207-07)	85 g	2025-12-03	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Lasolex AG (Miconazole Nitrate 2%) Antifungal Gel	Puretek Corporation	2025-12-31	HUMAN OTC DRUG LABEL	5