Home NDC 41250-386-30 Tolnaftate
Product NDC 41250-386
Requested package NDC 41250-386-30
11-digit product format 412500386
Labeler code 41250
Product ID 41250-386_f2049ac5-92fb-b5e2-e053-2995a90a3d59
Type HUMAN OTC DRUG
Nonproprietary name Anti-Fungal Liquid Maximum Strength
Dosage form LIQUID
Route TOPICAL
Labeler Meijer Distribution Inc.
Application part333C
Marketing category OTC MONOGRAPH FINAL
Marketing start 2021-04-06
Marketing end 0000-00-00
Substance TOLNAFTATE
Active strength 0 g/30mL
NDC exclude flag No
Listing certified through 2024-12-31
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 · 2 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 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 41250-386 41250-386-30 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 41250-386 41250-386-30 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41250-386 TOLNAFTATE (ANTI-FUNGAL LIQUID MAXIMUM STRENGTH) LIQUID [MEIJER DISTRIBUTION INC.] 4 Legacy NDC 20241016_bf4eacb0-4b91-c35e-e053-2995a90aee2f.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 41250-386-30 41250038630 30 mL in 1 BOTTLE, WITH APPLICATOR (41250-386-30) 30 ml 2021-04-06 0000-00-00 No No Current