hair regrowth treatment

Product NDC
30142-719
11-digit product format
301420719
Labeler code
30142
Product ID
30142-719_7214bcc4-79e5-4343-aa18-6075d5c45bab
Type
HUMAN OTC DRUG
Nonproprietary name
Minoxidil
Dosage form
AEROSOL, FOAM
Route
TOPICAL
Labeler
Kroger Company
Application
ANDA091344
Marketing category
ANDA
Marketing start
2018-05-22
Substance
MINOXIDIL
Active strength
50 mg/g
Pharmacologic classes
Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
hair regrowth treatment
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MINOXIDIL50 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii5965120SH1
Rxcui645146

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
30142-719-02hair regrowth treatment60 g in 1 CANAEROSOL, FOAM604
30142-719-02hair regrowth treatment2 in 1 CARTONAEROSOL, FOAM24

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
30142-719HAIR REGROWTH TREATMENT (MINOXIDIL) AEROSOL, FOAM [KROGER COMPANY]4Current NDC, Legacy NDC, 2 package rows20220311_1c9a23e0-d2c6-4de6-9fdb-28ffa38b9af0.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
645146minoxidil 5 % Topical FoamPSN1c9a23e0-d2c6-4de6-9fdb-28ffa38b9af04
645146minoxidil 50 MG/ML Topical FoamSCD1c9a23e0-d2c6-4de6-9fdb-28ffa38b9af04
645146minoxidil 5 % Topical FoamSY1c9a23e0-d2c6-4de6-9fdb-28ffa38b9af04

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
30142-719-02301420719022 CAN in 1 CARTON (30142-719-02) / 60 g in 1 CAN2 can2018-05-220000-00-00NoNoCurrent