SUPER WHITE STUFF Pain Relief

Product NDC
14448-445
11-digit product format
144480445
Labeler code
14448
Product ID
14448-445_0f9cff32-4c60-e95a-e063-6294a90a9707
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL
Dosage form
CREAM
Route
TOPICAL
Labeler
BLUE SPRING WELLNESS
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-03-04
Substance
MENTHOL
Active strength
14 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
SUPER WHITE STUFF Pain Relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL14 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiL7T10EIP3A
Rxcui2391332

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
14448-445-00SUPER WHITE STUFF Pain Relief118 mL in 1 JARCREAM1181

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
14448-445SUPER WHITE STUFF PAIN RELIEF (MENTHOL) CREAM [BLUE SPRING WELLNESS]1Current NDC, 1 package rows20240304_e6d27df5-118c-4c6d-86e8-7b4401a39c76.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2391332menthol 1.4 % Topical CreamPSNe6d27df5-118c-4c6d-86e8-7b4401a39c761
2391332menthol 14 MG/ML Topical CreamSCDe6d27df5-118c-4c6d-86e8-7b4401a39c761
2391332menthol 1.4 % Topical CreamSYe6d27df5-118c-4c6d-86e8-7b4401a39c761

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
14448-445-0014448044500118 mL in 1 JAR (14448-445-00) 118 ml2024-03-04NoNoHistorical