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# Observed captured status history: Rows come only from successfully parsed FDA auxiliary ZIP captures. They show the state present in that artifact, not a continuous regulatory timeline. Absence before, after, or between captures is not proof of status, and a known non-data HTTP 403 capture is preserved in backfill provenance but cannot produce a status row.
Historic NDC status page 1 of 1 · 9 matching rows.
Browse every current auxiliary row. · Browse the complete NDC auxiliary source catalog.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2022-08-30 03:57 UTC · source 2022-08-29 excluded product product 51414-904 I Inactivated by FDA excluded / ndc_excluded.zip fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 51414-904 51414-904-02 I Inactivated by FDA excluded / ndc_excluded.zip fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 51414-904 51414-904-01 I Inactivated by FDA excluded / ndc_excluded.zip fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product 51414-904 I Inactivated by FDA excluded / ndc_excluded.zip 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 51414-904 51414-904-02 I Inactivated by FDA excluded / ndc_excluded.zip 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 51414-904 51414-904-01 I Inactivated by FDA excluded / ndc_excluded.zip 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product 51414-904 I Inactivated by FDA excluded / ndc_excluded.zip bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 51414-904 51414-904-02 I Inactivated by FDA excluded / ndc_excluded.zip bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 51414-904 51414-904-01 I Inactivated by FDA excluded / ndc_excluded.zip bd6a592717d7…303034d00443…
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