Home NDC 58593-800-01 Ongo - Fin
Product NDC 58593-800
Requested package NDC 58593-800-01
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 · 1 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 58593-800 58593-800-01 I Inactivated by FDA excluded / ndc_excluded.zip 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 41 of 49 · 969 matching rows.
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