Home NDC 71320-200 miaderm-L
Product NDC 71320-200
11-digit product format 713200200
Labeler code 71320
Product ID 71320-200_af4ad992-a560-45f9-ba54-f393063aa420
Type HUMAN OTC DRUG
Nonproprietary name Lidocaine Hydrochloride
Dosage form LOTION
Route TOPICAL
Labeler Aiden Industries LLC
Application part348
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2015-08-13
Marketing end 0000-00-00
Substance LIDOCAINE HYDROCHLORIDE
Active strength 40 mg/mL
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 · 4 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 2020-12-18 03:04 UTC · source 2020-12-17 excluded product product e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 71320-200-06 e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 71320-200-06 9bebd1f3094a…5416666fcb17…
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 Units Marketing start Marketing end Sample Exclude flag Status 71320-200-06 71320020006 118 mL in 1 TUBE (71320-200-06) 118 ml 2018-09-11 0000-00-00 No No Current