Muscle Rub

Product NDC
70338-652
11-digit product format
703380652
Labeler code
70338
Product ID
70338-652_b76a758b-4dbd-961b-e053-2995a90ab04c
Type
HUMAN OTC DRUG
Nonproprietary name
Muscle Rub
Dosage form
CREAM
Route
TOPICAL
Labeler
MEDZONE PRODUCTS LLC
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2019-01-01
Marketing end
0000-00-00
Substance
MENTHOL
Active strength
35 mg/g
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70338-652-012022-01-28C16284748780-1d6a99b39-4d23-a426-e053-dadaa90af4c2Muscle Rub

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70338-652-01Muscle Rub85 g in 1 TUBECREAM852

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70338-652MUSCLE RUB CREAM [MEDZONE PRODUCTS LLC]2Legacy NDC, 1 package rows20201227_9b0c5de3-cfff-23db-e053-2995a90a27b4.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2000534menthol 3.5 % Topical CreamPSN9b0c5de3-cfff-23db-e053-2995a90a27b42
2000534menthol 35 MG/ML Topical CreamSCD9b0c5de3-cfff-23db-e053-2995a90a27b42
2000534menthol 3.5 % Topical CreamSY9b0c5de3-cfff-23db-e053-2995a90a27b42

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70338-652-017033806520185 g in 1 TUBE (70338-652-01) 85 g2019-01-010000-00-00NoNoCurrent