Medicated Body

Product NDC
58037-001
11-digit product format
580370001
Labeler code
58037
Product ID
58037-001_299ae5b5-bef2-3de8-e063-6394a90acf91
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL
Dosage form
POWDER
Route
TOPICAL
Labeler
New Pride Corp
Application
M016
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-09-01
Substance
MENTHOL
Active strength
.42 g/283g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Medicated Body
Brand name suffix
Powder
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL.42 g/283g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiL7T10EIP3A
Rxcui1431703

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58037-001-01Medicated BodyPowder283 g in 1 BOTTLEPOWDER2832

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58037-001MEDICATED BODY POWDER (MENTHOL) POWDER [NEW PRIDE CORP]2Current NDC, Legacy NDC, 1 package rows20241222_f0f0e332-cb93-42a7-e053-2995a90ac4ae.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1431703menthol 0.15 % Topical PowderPSNf0f0e332-cb93-42a7-e053-2995a90ac4ae2
1431703menthol 0.0015 MG/MG Topical PowderSCDf0f0e332-cb93-42a7-e053-2995a90ac4ae2
1431703menthol 0.15 % Topical PowderSYf0f0e332-cb93-42a7-e053-2995a90ac4ae2
1431703menthol 1.5 MG per GM Topical PowderSYf0f0e332-cb93-42a7-e053-2995a90ac4ae2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
58037-001-0158037000101283 g in 1 BOTTLE (58037-001-01) 283 g2020-09-010000-00-00NoNoCurrent