Home NDC 56104-040-03 Benzethonium chloride Plus Dyclonine hydrochloride
Product NDC 56104-040
Requested package NDC 56104-040-03
11-digit product format 561040040
Labeler code 56104
Product ID 56104-040_c74064c0-0e8a-4a5c-e053-2a95a90a1e86
Type HUMAN OTC DRUG
Nonproprietary name Liquid Bandage
Dosage form LIQUID
Route TOPICAL
Labeler Premier Brands of America Inc.
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2018-01-03
Marketing end 0000-00-00
Substance BENZETHONIUM CHLORIDE; DYCLONINE HYDROCHLORIDE
Active strength 0 mg/9mL; mg/9mL
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…
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 56104-040-03 56104004003 9 mL in 1 BOTTLE, WITH APPLICATOR (56104-040-03) 9 ml 2018-01-03 0000-00-00 No No Current