Home NDC 51414-903 GENUINE TRIPLE ANTIBIOTIC
Product NDC 51414-903
11-digit product format 514140903
Labeler code 51414
Product ID 51414-903_620623fa-140f-93d0-e053-2a91aa0aaebb
Type HUMAN OTC DRUG
Nonproprietary name bacitracin zinc,neomycin sulfate,polymyxin b sulfate
Dosage form OINTMENT
Route TOPICAL
Labeler Yuyao Jessie Commodity Co.,Ltd.
Application part333B
Marketing category OTC MONOGRAPH FINAL
Marketing start 2016-01-20
Marketing end 0000-00-00
Substance POLYMYXIN B SULFATE; BACITRACIN ZINC; NEOMYCIN SULFATE
Active strength 5000 [iU]/g; [iU]/g; mg/g
NDC exclude flag No
Listing certified through 2020-12-31
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, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2022-08-30 03:57 UTC · source 2022-08-29 excluded product product fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 51414-903-02 fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 51414-903-01 fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 51414-903-02 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 51414-903-01 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 51414-903-02 bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 51414-903-01 bd6a592717d7…303034d00443…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 51414-903-01 51414090301 .5 g in 1 PACKET (51414-903-01) 2018-01-05 0000-00-00 No No Current 51414-903-02 51414090302 .9 g in 1 PACKET (51414-903-02) 2018-01-05 0000-00-00 No No Current