SUPER WHITE STUFF Pain Relief

Product NDC
14448-306
11-digit product format
144480306
Labeler code
14448
Product ID
14448-306_09d6fabb-0d18-222e-e063-6294a90a95b6
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL
Dosage form
CREAM
Route
TOPICAL
Labeler
BLUE SPRING WELLNESS, L.L.C.
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-08-01
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
14448-306-40SUPER WHITE STUFF Pain Relief130 mL in 1 JARCREAM1304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
14448-306SUPER WHITE STUFF PAIN RELIEF (MENTHOL) CREAM [BLUE SPRING WELLNESS, L.L.C.]4Current NDC, Legacy NDC, 1 package rows20231111_9f948fb4-4275-4a1f-83f8-cd708db4a296.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2391332menthol 1.4 % Topical CreamPSN9f948fb4-4275-4a1f-83f8-cd708db4a2964
2391332menthol 14 MG/ML Topical CreamSCD9f948fb4-4275-4a1f-83f8-cd708db4a2964
2391332menthol 1.4 % Topical CreamSY9f948fb4-4275-4a1f-83f8-cd708db4a2964

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
14448-306-4014448030640130 mL in 1 JAR (14448-306-40) 130 ml2020-08-010000-00-00NoNoCurrent