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 46 of 49 · 973 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
MICONAZOLE Nitrate 2% Cream ANTIFUNGAL	MICONAZOLE NITRATE	ASTONEA LABS PRIVATE LIMITED	e66191a6-0c3c-7319-e053-2a95a90aae84	2024-06-25	Warnings	Exact identifier application number: M005
clotrimazole	CLOTRIMAZOLE	A-S Medication Solutions	b63a3fe5-5684-41bc-ad6c-69c54e5b942d	2024-06-20	Warnings	Exact identifier application number: M005
THERA Antifungal Body	MICONAZOLE NITRATE	McKesson Medical-Surgical Inc.	31096041-28c9-4b16-bbd1-dbadefd37505	2024-06-14	Warnings	Exact identifier application number: M005
Antifungal Body	MICONAZOLE NITRATE	McKesson	4fb9aece-0baa-475e-e054-00144ff8d46c	2024-06-13	Warnings	Exact identifier application number: M005
Secura Protective	ZINC OXIDE	Smith & Nephew Medical Ltd	b077aa64-49a3-42ee-abb3-88f833635b93	2024-06-12	Warnings	Exact identifier application number: M005
clotrimazole	CLOTRIMAZOLE	NuCare Pharmaceuticals,Inc.	627375fb-2f20-16bc-e053-2a91aa0a1542	2024-06-06	Warnings	Exact identifier application number: M005
Clotrimazole	CLOTRIMAZOLE	Cardinal Health 110 dba LEADER	199df107-3384-6e03-e063-6294a90afc38	2024-05-29	Warnings	Exact identifier application number: M005
Femmesil	CLOTRIMAZOLE	Aidance Skincare & Topical Solutions, LLC	efddad82-9dc7-4cd9-b33c-7e85f30d992e	2024-05-24	Warnings	Exact identifier application number: M005
Anti-Fungal	MICONAZOLE NITRATE	Universal Distribution Center LLC	8f316b0d-d308-4ae6-82c4-39bb0d1d474e	2024-05-21	Warnings	Exact identifier application number: M005
CANESPIES	TOLNAFTATE	OPMX LLC	e2f9eedc-3c43-416b-85b5-ba07fb5fb4db	2024-05-17	Warnings	Exact identifier application number: M005
Up and Up Antifungal	TOLNAFTATE 1%	Target Corporation	8f54c8c7-6771-49c3-b429-53aa6df54dc5	2024-05-08	Warnings	Exact identifier application number: M005
Up and Up Athletes Foot	CLOTRIMAZOLE 1%	Target Corporation	52b61859-11ae-4990-aa0c-9dc1dd00adf4	2024-05-08	Warnings	Exact identifier application number: M005
ADI Medical PVP-I Pouch, Foil	POVIDONE-IODINE	Asia Dynamics Inc., d/b/a ADI Medical	0e8baf24-0c67-5511-e063-6394a90acaa1	2024-05-02	Warnings	Exact identifier application number: M005
Caseys Antimicrobial Hand Sanitizer	ETHYL ALCOHOL	Navajo Manufacturing Company Inc.	78863024-390c-4ff9-8ed6-02af07902a30	2024-04-29	Warnings	Exact identifier application number: M005
MQUPIN Liquid Fungal Nail Treatment	LIQUID FUNGAL NAIL TREATMENT	Zhengzhou Miaoqi Medical Technology Co., Ltd.	14782f8c-3b29-1d88-e063-6294a90ac3e4	2024-03-25	Warnings	Exact identifier application number: M005
ETADERM Advanced Antifungal Support	UNDECYLENIC ACID	NUEPHASE LLC	adb12a1c-ece9-4a59-a62c-89d212c57e6f	2024-03-13	Warnings	Exact identifier application number: M005
Dermachange Jock	MICONAZOLE NITRATE	Private label Beauty and Wellness	12eef049-76c9-1450-e063-6394a90a00ea	2024-03-05	Warnings	Exact identifier application number: M005
Clotrimazole Antifungal	CLOTRIMAZOLE	Trifecta Pharmaceuticals USA, LLC.	11bf50db-552e-0a39-e063-6394a90af60d	2024-02-19	Warnings	Exact identifier application number: M005
TOLNAFTATE ANTIFUNGAL	TOLNAFTATE	Bryant Ranch Prepack	fbbd159c-217e-46d3-963c-ba0bd1e9bbe8	2024-01-29	Warnings	Exact identifier application number: M005
Target Jock Itch	CLOTRIMAZOLE 1%	Target Corporation	f44d4c44-99d1-413f-b9c3-8330bdd21abb	2024-01-17	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