Home NDC 68016-608-00 Tolnaftate
Product NDC 68016-608
Requested package NDC 68016-608-00
11-digit product format 680160608
Labeler code 68016
Product ID 68016-608_995ef84e-2ff0-efe8-e053-2a95a90a7c4d
Type HUMAN OTC DRUG
Nonproprietary name Antifungal Spray Powder
Dosage form AEROSOL, SPRAY
Route TOPICAL
Labeler Chain Drug Consortium, LLC
Application part333C
Marketing category OTC MONOGRAPH FINAL
Marketing start 2003-05-23
Marketing end 2021-02-26
Substance TOLNAFTATE
Active strength 0 g/130g
NDC exclude flag No
Listing certified through 0000-00-00
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 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded TOLNAFTATE ACTIVE INGREDIENT 06KB629TKV TOLNAFTATE (ANTIFUNGAL SPRAY POWDER) AEROSOL, SPRAY [CHAIN DRUG CONSORTIUM, LLC] 2 TOLNAFTATE ACTIVE MOIETY 06KB629TKV TOLNAFTATE (ANTIFUNGAL SPRAY POWDER) AEROSOL, SPRAY [CHAIN DRUG CONSORTIUM, LLC] 2 ALCOHOL INACTIVE INGREDIENT 3K9958V90M TOLNAFTATE (ANTIFUNGAL SPRAY POWDER) AEROSOL, SPRAY [CHAIN DRUG CONSORTIUM, LLC] 2 BUTYLATED HYDROXYTOLUENE INACTIVE INGREDIENT 1P9D0Z171K TOLNAFTATE (ANTIFUNGAL SPRAY POWDER) AEROSOL, SPRAY [CHAIN DRUG CONSORTIUM, LLC] 2 ISOBUTANE INACTIVE INGREDIENT BXR49TP611 TOLNAFTATE (ANTIFUNGAL SPRAY POWDER) AEROSOL, SPRAY [CHAIN DRUG CONSORTIUM, LLC] 2 PPG-12-BUTETH-16 INACTIVE INGREDIENT 58CG7042J1 TOLNAFTATE (ANTIFUNGAL SPRAY POWDER) AEROSOL, SPRAY [CHAIN DRUG CONSORTIUM, LLC] 2 TALC INACTIVE INGREDIENT 7SEV7J4R1U TOLNAFTATE (ANTIFUNGAL SPRAY POWDER) AEROSOL, SPRAY [CHAIN DRUG CONSORTIUM, LLC] 2
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 68016-608-00 68016060800 130 g in 1 CAN (68016-608-00) 130 g 2003-05-23 2021-02-26 No No Current