Home NDC 36800-075 Tolnaftate
Product NDC 36800-075
11-digit product format 368000075
Labeler code 36800
Product ID 36800-075_bd485f31-bd3e-3ae7-e053-2995a90a54f3
Type HUMAN OTC DRUG
Nonproprietary name Antifungal Liquid Maximum Strength
Dosage form LIQUID
Route TOPICAL
Labeler Topco Associates LLC
Application part333C
Marketing category OTC MONOGRAPH FINAL
Marketing start 2021-03-11
Marketing end 0000-00-00
Substance TOLNAFTATE
Active strength 0 g/30mL
NDC exclude flag No
Listing certified through 2022-12-31
Current FDA listing Historical FDA.report record 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 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 36800-075-01 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 36800-075-01 f5e01cc5f278…a2eaf40c39c3…
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 36800-075 TOLNAFTATE (ANTIFUNGAL LIQUID MAXIMUM STRENGTH) LIQUID [TOPCO ASSOCIATES LLC] 6 Legacy NDC 20241215_bd485f21-5a8a-7806-e053-2a95a90a35c8.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 36800-075-01 36800007501 30 mL in 1 BOTTLE, WITH APPLICATOR (36800-075-01) 30 ml 2021-03-11 0000-00-00 No No Current