Home NDC 11673-744 up and up lidocaine pain relief
Product NDC 11673-744
11-digit product format 116730744
Labeler code 11673
Product ID 11673-744_4a05261b-af63-46d1-a8b5-ec176ca1eba8
Type HUMAN OTC DRUG
Nonproprietary name lidocaine
Dosage form PATCH
Route PERCUTANEOUS; TOPICAL; TRANSDERMAL
Labeler Target Corporation
Application part348
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2019-07-15
Marketing end 0000-00-00
Substance LIDOCAINE
Active strength 560 mg/1
NDC exclude flag No
Listing certified through 2021-12-31
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 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 11673-744-91 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 11673-744-91 f5e01cc5f278…a2eaf40c39c3…
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 11673-744-91 11673074491 6 POUCH in 1 CARTON (11673-744-91) > 1 PATCH in 1 POUCH 6 pouch 2019-07-15 0000-00-00 No No Current