Home NDC 50066-623 Dragon Lidocaine Pain
Product NDC 50066-623
11-digit product format 500660623
Labeler code 50066
Product ID 50066-623_ee6c87d5-ba74-4305-9ef6-5f065222562d
Type HUMAN OTC DRUG
Nonproprietary name Lidocaine Hydrochloride
Dosage form CREAM
Route TOPICAL
Labeler Genomma Lab USA
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-09-15
Substance LIDOCAINE HYDROCHLORIDE
Active strength 40 mg/g
Pharmacologic classes Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Dragon Lidocaine Pain
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE HYDROCHLORIDE 40 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination V13007Z41A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1010895 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 18 of 147 · 2,937 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 50066-623-27 50066062327 1 TUBE in 1 CARTON (50066-623-27) / 76.5 g in 1 TUBE 1 tube 2026-09-15 No No Current