Home NDC 58593-800 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
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.
FDA-Initiated Inactive NDC Indexing# 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# 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 39 of 49 · 973 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Terrasil Anti-Fungal Treatment MAX CLOTRIMAZOLE Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions db356cc8-f473-4eb2-b8d8-72606fca9dc0 2025-05-23 Warnings Exact identifier application number: M005 terrasil Folliculitis Cream Maximum Strength CLOTRIMAZOLE Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions 35d54756-00dd-bbe1-e063-6394a90a9e02 2025-05-23 Warnings Exact identifier application number: M005 Paume Moisturizing Antibacterial Hand Gel ALCOHOL Paume Inc b6fe12bf-6430-5861-e053-2a95a90a6c8f 2025-05-22 Warnings Exact identifier application number: M005 Tolnaftate Cream 1% ANTIFUNGAL TOLNAFTATE Trifecta Pharmaceuticals Usa Llc 96a40ccd-17f7-4e4e-98da-207802fa2b2d 2025-05-15 Warnings Exact identifier application number: M005 MICONAZOLE Nitrate 2% Cream ANTIFUNGAL MICONAZOLE NITRATE Cardinal Health 110 dba LEADER 34f4c733-2eb2-0db0-e063-6394a90a6431 2025-05-13 Warnings Exact identifier application number: M005 Dr CANUSO fungal nail eraser TOLNAFTATE OIL Renu Laboratories, LLC 2083f9ed-09d6-26e6-e054-00144ff88e88 2025-05-13 Warnings Exact identifier application number: M005 Dr. Canuso foot repair serum TOLNAFTATE SERUM Renu Laboratories, LLC 1fcc52c5-7030-13cb-e054-00144ff8d46c 2025-05-13 Warnings Exact identifier application number: M005 Private Label Antifungal Barrier Cream MICONAZOLE NITRATE ANTIFUNGAL CREAM Swiss-American CDMO, LLC 2ee40c37-504b-43ed-960a-535015407492 2025-05-09 Warnings Exact identifier application number: M005 Osimoon Fungal Nail Treatment Kit OSIMOON FUNGAL NAIL TREATMENT KIT Guangzhou Zanming Trading Co., Ltd. 34aec10d-a0d0-d956-e063-6394a90a39b2 2025-05-09 Warnings Exact identifier application number: M005 ANTIFUNGAL MICONAZOLE VIVE HEALTH LLC 33d9c724-d4c4-2597-e063-6294a90aa5f3 2025-04-28 Warnings Exact identifier application number: M005 ANTIFUNGAL CLOTRIMAZOLE VIVE HEALTH LLC 33db98f5-f6d9-742a-e063-6394a90a2a03 2025-04-28 Warnings Exact identifier application number: M005 Foot Cure Nail Repair Pen ANTIFUNGAL NAIL REPAIR PEN SANSAR, LLC 9c823e27-8bb3-4ccd-bf7e-a99d45908e88 2025-04-25 Warnings Exact identifier application number: M005 WISH HAND SANITIZER CUCUMBER MELON ALCOHOL HAND SANITIZER PT SUPER HOME PRODUCT INDONESIA 3380404d-9499-e9fb-e063-6394a90a0f27 2025-04-24 Warnings Exact identifier application number: M005 WISH HAND SANITIZER SWEET GUAVA FRESH COCONUT ALCOHOL HAND SANITIZER PT SUPER HOME PRODUCT INDONESIA 3380fe6d-e059-401a-e063-6394a90a787a 2025-04-24 Warnings Exact identifier application number: M005 WISH HAND SANITIZER DRAGONFRUIT JASMINE ALCOHOL HAND SANITIZER PT SUPER HOME PRODUCT INDONESIA 3381cefb-281c-9b85-e063-6294a90acfd9 2025-04-24 Warnings Exact identifier application number: M005 Wish Hand Sanitizer Coconut Cream White Florals ALCOHOL HAND SANITIZER PT SUPER HOME PRODUCT INDONESIA 33826aef-6e50-2730-e063-6394a90a727b 2025-04-24 Warnings Exact identifier application number: M005 WISH HAND SANITIZER GOLDEN CITRUS ALCOHOL HAND SANITIZER PT SUPER HOME PRODUCT INDONESIA 3391a78e-525d-c2ba-e063-6394a90a1e99 2025-04-24 Warnings Exact identifier application number: M005 WISH HAND SANITIZER SALTED CARAMEL PISTACHIO ALCOHOL HAND SANITIZER PT SUPER HOME PRODUCT INDONESIA 33927939-a9dc-ab67-e063-6394a90a71cc 2025-04-24 Warnings Exact identifier application number: M005 WISH HAND SANITIZER BLACK PLUM VANILLA ALCOHOL HAND SANITIZER PT. SUPER HOME PRODUCT INDONESIA 336c751f-6a33-ca55-e063-6394a90a9749 2025-04-23 Warnings Exact identifier application number: M005 WISH HAND SANITIZER VIOLET ORCHID SANDALWOOD ALCOHOL HAND SANITIZER PT. SUPER HOME PRODUCT INDONESIA 337e4526-238a-bc2d-e063-6394a90a5a27 2025-04-23 Warnings Exact identifier application number: M005
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