COOL BREEZE Pain Relief

Product NDC
72744-433
11-digit product format
727440433
Labeler code
72744
Product ID
72744-433_09135640-d8a9-790c-e063-6294a90a8fce
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL
Dosage form
GEL
Route
TOPICAL
Labeler
COOL BREEZE US LLC
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-11-13
Substance
MENTHOL
Active strength
51 mg/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL51 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiL7T10EIP3A
Rxcui2669723

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72744-433-00COOL BREEZE Pain Relief118 mL in 1 TUBEGEL1181

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72744-433COOL BREEZE PAIN RELIEF (MENTHOL) GEL [COOL BREEZE US LLC]1Current NDC, 1 package rows20231114_14dcf4ee-6778-49d4-8601-9205737432ea.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2669723menthol 5.1 % Topical GelPSN14dcf4ee-6778-49d4-8601-9205737432ea1
2669723menthol 0.051 MG/MG Topical GelSCD14dcf4ee-6778-49d4-8601-9205737432ea1
2669723menthol 5.1 % Topical GelSY14dcf4ee-6778-49d4-8601-9205737432ea1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72744-433-0072744043300118 mL in 1 TUBE (72744-433-00) 118 ml2023-11-13NoNoCurrent