Home NDC 63742-013 Lightning Pain Relief
Product NDC 63742-013
11-digit product format 637420013
Labeler code 63742
Product ID 63742-013_4c143af2-cd3f-2fc8-e063-6394a90a40b7
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL
Dosage form CREAM
Route TOPICAL
Labeler Clinical Resolution Laboratory, Inc.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-05-01
Substance MENTHOL
Active strength 40 mg/g
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 Lightning Pain Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 40 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1148430 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 63742-013-00 Lightning Pain Relief 65 g in 1 BOTTLE CREAM 65 5 63742-013-01 Lightning Pain Relief 101 g in 1 BOTTLE CREAM 101 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63742-013 LIGHTNING PAIN RELIEF (MENTHOL) CREAM [CLINICAL RESOLUTION LABORATORY, INC.] 4 Current NDC, Legacy NDC, 2 package rows 20240103_80af21f5-dba8-42b0-8a65-ac5a94d83ca8.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 151 · 3,020 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 63742-013-00 63742001300 65 g in 1 BOTTLE (63742-013-00) 65 g 2019-05-01 0000-00-00 No No Current 63742-013-01 63742001301 101 g in 1 BOTTLE (63742-013-01) 101 g 2019-05-01 0000-00-00 No No Current