Ongo - Fin

Product NDC: 58593-800
11-digit product format: 585930800
Labeler code: 58593
Product ID: 58593-800_24708234-0886-bb16-e063-6294a90a6898
Type: HUMAN OTC DRUG
Nonproprietary name: TOLNAFTATE
Dosage form: LIQUID
Route: TOPICAL
Labeler: Efficient Laboratories Inc.
Application: M005
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2004-02-01
Substance: TOLNAFTATE
Active strength: 1 mg/100mL
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	58593-800	58593-800-02	D	Discontinued by firm		2026-10-12

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 15 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	58593-800-02	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	58593-800-02	D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	58593-800-02	D	Discontinued by firm	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	58593-800-02	D	Discontinued by firm	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	58593-800-02	D	Discontinued by firm	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	58593-800-02	D	Discontinued by firm	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	58593-800-02	D	Discontinued by firm	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	58593-800-02	D	Discontinued by firm	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	58593-800-02	D	Discontinued by firm	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	58593-800-02	D	Discontinued by firm	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	58593-800-02	D	Discontinued by firm	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	58593-800-02	D	Discontinued by firm	`557ba5c1ecfa…`	`9c80585c8c6e…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded product	product		I	Inactivated by FDA	`110d247fa046…`	`a55b01930146…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded package	package	58593-800-02	I	Inactivated by FDA	`110d247fa046…`	`a55b01930146…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded package	package	58593-800-01	I	Inactivated by FDA	`110d247fa046…`	`a55b01930146…`

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: Ongo - Fin
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
TOLNAFTATE	1 mg/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
06KB629TKV	Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
bb5fb71f-bee0-42fa-9c9f-6231b555324c	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
58593-800-01	2020-02-19	Drud Facts
58593-800-02	2020-02-19	Drud Facts
58593-800-01	2019-10-29	Drud Facts
58593-800-02	2019-10-29	Drud Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
58593-800-01	Ongo - Fin	30 mL in 1 BOTTLE, WITH APPLICATOR	LIQUID	30		8
58593-800-02	Ongo - Fin	30 mL in 1 BOTTLE, SPRAY	LIQUID	30		8

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
TOLNAFTATE	ACTIVE INGREDIENT	06KB629TKV	ONGO - FIN (TOLNAFTATE) LIQUID [EFFICIENT LABORATORIES INC.]	1
TOLNAFTATE	ACTIVE MOIETY	06KB629TKV	ONGO - FIN (TOLNAFTATE) LIQUID [EFFICIENT LABORATORIES INC.]	1
ACETONE	INACTIVE INGREDIENT	1364PS73AF	ONGO - FIN (TOLNAFTATE) LIQUID [EFFICIENT LABORATORIES INC.]	1
ALOE VERA LEAF	INACTIVE INGREDIENT	ZY81Z83H0X	ONGO - FIN (TOLNAFTATE) LIQUID [EFFICIENT LABORATORIES INC.]	1
ALPHA-TOCOPHEROL	INACTIVE INGREDIENT	H4N855PNZ1	ONGO - FIN (TOLNAFTATE) LIQUID [EFFICIENT LABORATORIES INC.]	1
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	ONGO - FIN (TOLNAFTATE) LIQUID [EFFICIENT LABORATORIES INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	ONGO - FIN (TOLNAFTATE) LIQUID [EFFICIENT LABORATORIES INC.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
58593-800	ONGO - FIN (TOLNAFTATE) LIQUID [EFFICIENT LABORATORIES INC.]	8	Current NDC, Legacy NDC, 2 package rows	20241016_bb5fb71f-bee0-42fa-9c9f-6231b555324c.zip

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 43 of 49 · 973 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Clotrimazole	DRS. CLOTRIMAZOLE	OL PHARMA TECH,LLC	b0e9fc77-6d5c-2472-e053-2995a90a3de4	2025-01-09	Warnings	Exact identifier application number: M005
Anti-Bacterial Wipes	BENZALKONIUM CHLORIDE	Tongling Jieya Biological Technology Co., Ltd.	d7aeb18f-abf2-49bd-a8a3-ac57f60fbe7d	2025-01-04	Warnings	Exact identifier application number: M005
AVON HeXashield Athletes Foot Cream	TOLNAFTATE	Tai Guk Pharm. Co., Ltd.	8f2b6a09-8cb0-0d17-e053-2995a90aa07f	2025-01-01	Warnings	Exact identifier application number: M005
Tolnaftate	TOLNAFTATE 1%	Trifecta Pharmaceuticals USA, LLC	091b907f-544a-86c9-e063-6294a90a5d87	2024-12-31	Warnings	Exact identifier application number: M005
terrasil Fungal Treatment	CLOTRIMAZOLE	Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions	278290f9-be14-81a8-e063-6294a90ad8cc	2024-12-26	Warnings	Exact identifier application number: M005
DEO PEDICO ABOVE NEYMAR JR MEN	DEO PEDICO ABOVE NEYMAR JR MEN	BASTON INDUSTRIA DE AEROSSOIS LTDA	ed4a9844-f20b-da5d-e053-2995a90adc09	2024-12-26	Warnings	Exact identifier application number: M005
Vite20	MICONAZOLE NITRATE	Blaine Labs Inc.	28a8d0dd-aab9-44ff-bab6-7ec4b5036a71	2024-12-24	Warnings	Exact identifier application number: M005
Vite20	UNDECYLENIC ACID	Blaine Labs Inc.	18f8ea1c-360e-43c0-98df-5816af4dec66	2024-12-24	Warnings	Exact identifier application number: M005
Tolnaftate Cream 1% ANTIFUNGAL	FAMILY WELLNESS TOLNAFTATE	Trifecta Pharmaceuticals USA, LLC	915759af-0d7f-6a87-e053-2a95a90acbd6	2024-12-20	Warnings	Exact identifier application number: M005
Rugby Clotrimazole Antifungal Cream	CLOTRIMAZOLE	Rugby Laboratories	a1365bc7-b376-adca-e053-2a95a90acf19	2024-12-20	Warnings	Exact identifier application number: M005
Miconazole Nitrate	ANTIFUNGAL MICONAZOLE POWDER SPRAY	Premier Brands of America Inc.	dc7a23bb-b246-89b1-e053-2995a90a9f2d	2024-12-20	Warnings	Exact identifier application number: M005
Warrior Antifungal Foot	MICONAZOLE NITRATE 2%	Derma Care Research Labs, LLC	cf2e9dc1-275b-4454-e053-2995a90af295	2024-12-20	Warnings	Exact identifier application number: M005
Tolnaftate Cream 1%	TOLNAFTATE	Pharmacy Value Alliance, LLC.	3abfd734-229b-1a0e-e054-00144ff88e88	2024-12-20	Warnings	Exact identifier application number: M005
Dermatool Fungal Nail Treatment	TOLNAFTATE 1%	Derma Care Research Labs, LLC	fbc1a55e-b994-4962-e053-6394a90a13ba	2024-12-19	Warnings	Exact identifier application number: M005
Novonail Solution	TOLNAFTATE 1%	Derma Care Research Labs, LLC	013d6107-e3b0-0264-e063-6394a90ae1e2	2024-12-19	Warnings	Exact identifier application number: M005
MICONAZOLE Nitrate 2% Cream ANTIFUNGAL	MICONAZOLE NITRATE	Rugby	f420de00-408f-9a2c-e053-2995a90adced	2024-12-17	Warnings	Exact identifier application number: M005
Relispray Antifungal Liquid	TOLNAFTATE	Midas-Care Pharmaceuticals Pvt. Ltd.	6522ad59-f810-408c-a9f9-9359d79302ce	2024-12-17	Warnings	Exact identifier application number: M005
Clotrimazole	FAMILY WELLNESS CLOTRIMAZOLE	Trifecta Pharmaceuticals USA LLC	915759af-0d7b-6a87-e053-2a95a90acbd6	2024-12-13	Warnings	Exact identifier application number: M005
Blistex Odor-Eaters Powder	TOLNAFTATE	Blistex Inc	819edb2f-dda7-45c3-b0da-ebcae354154e	2024-12-12	Warnings	Exact identifier application number: M005
Walgreens Athletes Foot	TOLNAFTATE SPRAY	Walgreens	c68ad65d-b016-0069-e053-2995a90ae7ef	2024-12-11	Warnings	Exact identifier application number: M005

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
06KB629TKV	TOLNAFTATE	2398-96-1	TOLNAFTATE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
58593-800-01	58593080001	30 mL in 1 BOTTLE, WITH APPLICATOR (58593-800-01)	30 ml	2004-02-01	0000-00-00	No	No	Current
58593-800-02	58593080002	30 mL in 1 BOTTLE, SPRAY (58593-800-02)	30 ml	2004-02-01	0000-00-00	No	No	Current