OLIVITA 5% Minoxidil

Product NDC
83818-028
11-digit product format
838180028
Labeler code
83818
Product ID
83818-028_4acbdf3d-976b-2cba-e063-6294a90a35e6
Type
HUMAN OTC DRUG
Nonproprietary name
5% Minoxidil
Dosage form
SOLUTION
Route
TOPICAL
Labeler
Shenzhen Xinxin Yunhai Technology Co., Ltd.
Application
M032
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2026-02-15
Substance
MINOXIDIL
Active strength
5 g/100mL
Pharmacologic classes
Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
OLIVITA 5% Minoxidil
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MINOXIDIL5 g/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii5965120SH1
Rxcui311724

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83818-028-01OLIVITA 5% Minoxidil2 in 1 BOXSOLUTION21
83818-028-01OLIVITA 5% Minoxidil60 mL in 1 BOTTLESOLUTION601

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311724minoxidil 5 % Topical SolutionPSN4acbdf3d-976a-2cba-e063-6294a90a35e61
311724minoxidil 50 MG/ML Topical SolutionSCD4acbdf3d-976a-2cba-e063-6294a90a35e61
311724minoxidil 3 GM per 60 ML Topical SolutionSY4acbdf3d-976a-2cba-e063-6294a90a35e61
311724minoxidil 5 % Topical SolutionSY4acbdf3d-976a-2cba-e063-6294a90a35e61
311724minoxidil 5 GM per 100 ML Topical SolutionSY4acbdf3d-976a-2cba-e063-6294a90a35e61

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
83818-028-01838180028012 BOTTLE in 1 BOX (83818-028-01) / 60 mL in 1 BOTTLE2 bottle2026-02-15NoNoHistorical