Home NDC 56104-008-04 Tolnaftate
Product NDC 56104-008
Requested package NDC 56104-008-04
11-digit product format 561040008
Labeler code 56104
Product ID 56104-008_c7045d71-6ba2-59f1-e053-2995a90a7c8d
Type HUMAN OTC DRUG
Nonproprietary name Foot Odor Control Spray Powder
Dosage form AEROSOL, POWDER
Route TOPICAL
Labeler Premier Brands of America Inc.
Application part333C
Marketing category OTC MONOGRAPH FINAL
Marketing start 2013-01-01
Marketing end 0000-00-00
Substance TOLNAFTATE
Active strength 1 g/113g
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 · 9 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…
DailyMed Socrata Ingredients# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 56104-008-04 56104000804 113 g in 1 CANISTER (56104-008-04) 113 g 2013-01-01 0000-00-00 No No Current