Home NDC 84019-042 Dr Wellskin Numbing Cream
Product NDC 84019-042
11-digit product format 840190042
Labeler code 84019
Product ID 84019-042_482f25cc-dee4-c3b6-e063-6294a90a8674
Type HUMAN OTC DRUG
Nonproprietary name 4% Lidocaine
Dosage form CREAM
Route TOPICAL
Labeler Shengnan (Guangzhou) Cosmetics Co., LTD
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-12
Substance LIDOCAINE
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 Dr Wellskin Numbing Cream
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE 40 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 98PI200987 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 84019-042-01 Dr Wellskin Numbing Cream 30 g in 1 BOTTLE CREAM 30 1
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 8 of 156 · 3,115 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 84019-042-01 84019004201 30 g in 1 BOTTLE (84019-042-01) 30 g 2026-01-12 No No Current