Home NDC 50804-955 Good Sense Burn Relief Aloe
Product NDC 50804-955
11-digit product format 508040955
Labeler code 50804
Product ID 50804-955_295758f2-3535-3e65-e063-6294a90a3948
Type HUMAN OTC DRUG
Nonproprietary name Lidocaine HCl
Dosage form GEL
Route TOPICAL
Labeler Geiss, Destin & Dunn, Inc
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-12-04
Substance LIDOCAINE HYDROCHLORIDE
Active strength .5 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 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 Good Sense Burn Relief Aloe
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE HYDROCHLORIDE .5 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 1011849 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 50804-955-08 Good Sense Burn Relief Aloe 227 g in 1 BOTTLE, PLASTIC GEL 227 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50804-955 GOOD SENSE BURN RELIEF ALOE (LIDOCAINE HCL) GEL [GEISS, DESTIN & DUNN, INC] 3 Current NDC, Legacy NDC, 1 package rows 20241217_b5a7f629-a88d-b49d-e053-2995a90a49fa.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 18 of 153 · 3,057 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 50804-955-08 50804095508 227 g in 1 BOTTLE, PLASTIC (50804-955-08) 227 g 2020-12-04 0000-00-00 No No Current