Home NDC 51414-904 GENUINE FIRST AID BURN ANTISEPTIC PAIN RELIEF WITH ALOE
Product NDC 51414-904
11-digit product format 514140904
Labeler code 51414
Product ID 51414-904_6207329a-5211-cbcf-e053-2a91aa0a719d
Type HUMAN OTC DRUG
Nonproprietary name benzalkonium chloride, lidocaine
Dosage form CREAM
Route TOPICAL
Labeler Yuyao Jessie Commodity Co.,Ltd.
Application part348
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2016-01-20
Marketing end 0000-00-00
Substance LIDOCAINE HYDROCHLORIDE; BENZALKONIUM CHLORIDE
Active strength 1 g/100g; g/100g
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 51414-904-02 fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 51414-904-01 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 51414-904-02 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 51414-904-01 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 51414-904-02 bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 51414-904-01 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 51414-904-01 51414090401 .5 g in 1 PACKET (51414-904-01) 2018-01-05 0000-00-00 No No Current 51414-904-02 51414090402 .9 g in 1 PACKET (51414-904-02) 2018-01-05 0000-00-00 No No Current