Lightning Pain Relief

Product NDC
72654-013
11-digit product format
726540013
Labeler code
72654
Product ID
72654-013_36edbc3f-501d-c1ea-e063-6394a90af6af
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol
Dosage form
CREAM
Route
TOPICAL
Labeler
Ebanel Laboratories, Inc
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-06-06
Substance
MENTHOL
Active strength
40 mg/g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Lightning Pain Relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL40 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiL7T10EIP3A
Rxcui1148430

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72654-013-00Lightning Pain Relief65 g in 1 BOTTLE, PLASTICCREAM651
72654-013-01Lightning Pain Relief101 g in 1 BOTTLE, PLASTICCREAM1011

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1148430menthol 4 % Topical CreamPSN36edbc3f-501c-c1ea-e063-6394a90af6af1
1148430menthol 40 MG/ML Topical CreamSCD36edbc3f-501c-c1ea-e063-6394a90af6af1
1148430menthol 4 % Topical CreamSY36edbc3f-501c-c1ea-e063-6394a90af6af1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72654-013-007265400130065 g in 1 BOTTLE, PLASTIC (72654-013-00) 65 g2025-06-06NoNoHistorical
72654-013-0172654001301101 g in 1 BOTTLE, PLASTIC (72654-013-01) 101 g2025-06-06NoNoHistorical