LidoPro

Product NDC
80425-0582
Type
HUMAN OTC DRUG
Nonproprietary name
lidocaine and menthol
Dosage form
PATCH
Route
TRANSDERMAL
Labeler
Advanced Rx of Tennessee, LLC
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Substance
LIDOCAINE; MENTHOL
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
80425-0582-130 POUCH in 1 CARTON (80425-0582-1) / 1 PATCH in 1 POUCH / 10 g in 1 PATCH2026-04-17NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
LidoPro PatchAdvanced Rx of Tennessee, LLC2026-04-17HUMAN OTC DRUG LABEL1