Regenpure Precision

Product NDC
71290-813
Type
HUMAN OTC DRUG
Nonproprietary name
MINOXIDIL
Dosage form
LIQUID
Route
TOPICAL
Labeler
Salonceuticals, Inc.
Application
ANDA076239
Marketing category
ANDA
Substance
MINOXIDIL
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
71290-813-021 BOTTLE in 1 BOX (71290-813-02) / 60 mL in 1 BOTTLE2017-03-05NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Regenpure Precision MinoxidilSalonceuticals, Inc.2017-03-06HUMAN OTC DRUG LABEL1