Home NDC 24330-240 SunBurnt PLUS Pain Relief
Product NDC 24330-240
11-digit product format 243300240
Labeler code 24330
Product ID 24330-240_cd41cc55-ae90-4c02-a405-cc81cd06ce2e
Type HUMAN OTC DRUG
Nonproprietary name Lidocaine Hydrochloride
Dosage form GEL
Route TOPICAL
Labeler Welmedix LLC dba Welmedix Consumer Healthcare
Application part348
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2018-03-15
Substance LIDOCAINE HYDROCHLORIDE
Active strength 1 g/100g
Pharmacologic classes Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base SunBurnt PLUS Pain Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE HYDROCHLORIDE 1 g/100g
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 1012204 Internal RxNorm 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 24330-240-01 SunBurnt PLUS Pain Relief 142 g in 1 TUBE GEL 142 1 24330-240-01 SunBurnt PLUS Pain Relief 1 in 1 CARTON GEL 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 24330-240 SUNBURNT PLUS PAIN RELIEF (LIDOCAINE HYDROCHLORIDE) GEL [WELMEDIX LLC DBA WELMEDIX CONSUMER HEALTHCARE] 1 Current NDC, Legacy NDC, 2 package rows 20180315_6363c695-f801-407d-a4e1-b0d9cfa0a273.zip
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 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 24330-240-01 24330024001 1 TUBE in 1 CARTON (24330-240-01) / 142 g in 1 TUBE 1 tube 2018-03-15 0000-00-00 No No Current