Rootly Hair Regrowth Treatment for Women

Product NDC
70150-004
11-digit product format
701500004
Labeler code
70150
Product ID
70150-004_ca315aa1-c1e6-686c-e053-2995a90acaaa
Type
HUMAN OTC DRUG
Nonproprietary name
Minoxidil 2%
Dosage form
SOLUTION
Route
TOPICAL
Labeler
TTEM, LLC
Application
ANDA078176
Marketing category
ANDA
Marketing start
2021-08-22
Marketing end
0000-00-00
Substance
MINOXIDIL
Active strength
2 g/100mL
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70150-004-012025-01-30C16284748780-12cef2736-9566-d83d-e063-dadaa90ab31fRootly Hair Regrowth Treatment 2% Minoxidil

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70150-004-01Rootly Hair Regrowth Treatment for Women60 mL in 1 BOTTLESOLUTION602
70150-004-01Rootly Hair Regrowth Treatment for Women1 in 1 BOXSOLUTION12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70150-004ROOTLY HAIR REGROWTH TREATMENT FOR WOMEN (MINOXIDIL 2%) SOLUTION [TTEM, LLC]2Legacy NDC, 2 package rows20230119_ca315aa1-c1e5-686c-e053-2995a90acaaa.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311723minoxidil 2 % Topical SolutionPSNca315aa1-c1e5-686c-e053-2995a90acaaa2
311723minoxidil 20 MG/ML Topical SolutionSCDca315aa1-c1e5-686c-e053-2995a90acaaa2
311723minoxidil 2 % Topical SolutionSYca315aa1-c1e5-686c-e053-2995a90acaaa2
311723minoxidil 2 GM per 100 ML Topical SolutionSYca315aa1-c1e5-686c-e053-2995a90acaaa2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70150-004-01701500004011 BOTTLE in 1 BOX (70150-004-01) > 60 mL in 1 BOTTLE1 bottle2021-08-220000-00-00NoNoCurrent