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 44 of 49 · 973 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Dr. Rainer s Vaginal Cream	MICONAZOLE NITRATE	Plexoris Health Care Products, Llc	1f0ee635-c70d-4194-a01d-370ca5c22fcd	2024-12-11	Warnings	Exact identifier application number: M005
BOA VIDA Antifungal	MICONAZOLE NITRATE	Central Solutions Inc	69c5340d-9abd-43bf-a90b-9568d615f06f	2024-12-09	Warnings	Exact identifier application number: M005
BLUESEA DISPOSABLE HAND SANITIZER	ALCOHOL	BLUE SEA AEROSOL & DAILY CARE CO., LTD	7a552be2-a9e1-4c6f-b1c2-79113a73bd2f	2024-12-06	Warnings	Exact identifier application number: M005
U HAND SANITIZER CLASSIC	BENZALKONIUM CHLORIDE	BLUE SEA AEROSOL & DAILY CARE CO., LTD	fbc27a24-0e81-4907-b24f-881c4fe0ec44	2024-12-06	Warnings	Exact identifier application number: M005
BLUESEA INSTANT HAND SANITIZER	ALCOHOL	BLUE SEA AEROSOL & DAILY CARE CO., LTD	e6b5ce49-d6d6-4b24-8b40-bfb1fb7005bd	2024-12-06	Warnings	Exact identifier application number: M005
Povidone-Iodine	POVIDONE-IODINE	Mazza Healthcare, LLC	31df570a-35ae-41a2-b04a-fce65e9d596d	2024-11-21	Warnings	Exact identifier application number: M005
Povidone-Iodine	POVIDONE-IODINE	Mazza Healthcare, LLC	3dc3303f-54b2-4aec-8568-5e0f8eb7cb14	2024-11-21	Warnings	Exact identifier application number: M005
WINCO ANTIFUNGAL	TOLNAFTATE 1%	WinCo Foods LLC	46b58c71-d62e-4b3d-b2ec-65407032eeea	2024-11-21	Warnings	Exact identifier application number: M005
Dynarex Antifungal	ANTIFUNGAL	Dynarex Corporation	ab5b6467-c158-4407-9d52-3c0731030680	2024-11-20	Warnings	Exact identifier application number: M005
Terrasil JockItch Treatment Maximum Strength	CLOTRIMAZOLE	Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions	8afe11c1-0a85-4255-8eba-e8cbde0759a0	2024-11-20	Warnings	Exact identifier application number: M005
Terrasil Ringworm Treatment MAX	CLOTRIMAZOLE	Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions	fc2b740a-49c1-4a01-a94c-8cade52a2b82	2024-11-20	Warnings	Exact identifier application number: M005
MICONAZOLE NITRATE	MICONAZOLE NITRATE	ALLIED TRADE LINK LLC	25520dba-0159-2a3f-e063-6294a90a4c33	2024-11-12	Warnings	Exact identifier application number: M005
CLOTRIMAZOLE	CLOTRIMAZOLE	ALLIED TRADE LINK LLC	266d7b94-2954-4831-e063-6394a90a3f33	2024-11-08	Warnings	Exact identifier application number: M005
Antifungal	TOLNAFTATE 1%	Chain Drug Marketing Association Inc.	26303499-dc58-f417-e063-6394a90a0a1b	2024-11-05	Warnings	Exact identifier application number: M005
AZOLEN	MICONAZOLE NITRATE	STRATUS PHARMACEUTICALS INC	3264bd0a-c628-404b-8c09-8586682d054e	2024-10-31	Warnings	Exact identifier application number: M005
BACITRACIN ZINC	BACITRACIN ZINC	STRATUS PHARMACEUTICALS INC	b2cb3a96-b0ca-42ee-8056-91d5450fb376	2024-10-31	Warnings	Exact identifier application number: M005
Premier Value Antifungal Maximum Strength	UNDECYLENIC ACID	PHARMACY VALUE ALLIANCE, LLC	f5694ee5-616c-40f6-8da4-c3620dbcd6f7	2024-10-28	Warnings	Exact identifier application number: M005
Clotrimazole 1%	CLOTRIMAZOLE	Chain Drug Marketing Association Inc.	24ff5ad7-2ff9-b254-e063-6394a90a27a7	2024-10-21	Warnings	Exact identifier application number: M005
Micomitin Antifungal	TOLNAFTATE	PureTek Corporation	de9842ba-0254-8ae1-e053-2995a90a0664	2024-10-16	Warnings	Exact identifier application number: M005
Ongo - Fin	TOLNAFTATE	Efficient Laboratories Inc.	bb5fb71f-bee0-42fa-9c9f-6231b555324c	2024-10-14	Warnings	Exact identifier application number: M005 ndc (product): 58593-800

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