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NDC 69968-0030-01 Womens Rogaine Unscented 50 mg/g Details

Womens Rogaine Unscented 50 mg/g

Womens Rogaine Unscented is a TOPICAL AEROSOL, FOAM in the HUMAN OTC DRUG category. It is labeled and distributed by Johnson & Johnson Consumer Inc.. The primary component is MINOXIDIL.

MedlinePlus Drug Summary

Minoxidil is used with other medications to treat high blood pressure. It is in a class of medications called vasodilators. It works by relaxing the blood vessels so that blood can flow more easily through the body. High blood pressure is a common condition and when not treated, can cause damage to the brain, heart, blood vessels, kidneys and other parts of the body. Damage to these organs may cause heart disease, a heart attack, heart failure, stroke, kidney failure, loss of vision, and other problems. In addition to taking medication, making lifestyle changes will also help to control your blood pressure. These changes include eating a diet that is low in fat and salt, maintaining a healthy weight, exercising at least 30 minutes most days, not smoking, and using alcohol in moderation.

Related Packages: 69968-0030-01
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Minoxidil

Minoxidil is used to stimulate hair growth and to slow balding. It is most effective for people under 40 years of age whose hair loss is recent. Minoxidil has no effect on receding hairlines. It does not cure baldness; most new hair is lost within a few months after the drug is stopped.

Related Packages: 69968-0030-01
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Minoxidil Topical

Product Information

NDC	69968-0030
Product ID	69968-0030_ee3348ed-b763-f3dc-e053-2a95a90a36ce
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Womens Rogaine Unscented
Proprietary Name Suffix	n/a
Non-Proprietary Name	Minoxidil
Product Type	HUMAN OTC DRUG
Dosage Form	AEROSOL, FOAM
Route	TOPICAL
Active Ingredient Strength	50
Active Ingredient Units	mg/g
Substance Name	MINOXIDIL
Labeler Name	Johnson & Johnson Consumer Inc.
Pharmaceutical Class	Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
DEA Schedule	n/a
Marketing Category	NDA
Application Number	NDA021812
Listing Certified Through	2024-12-31

Package

NDC 69968-0030-01 (69968003001)

Pricing Information	N/A
NDC Package Code	69968-0030-1
Billing NDC	69968003001
Package	1 CAN in 1 CARTON (69968-0030-1) / 60 g in 1 CAN
Marketing Start Date	2011-04-01
NDC Exclude Flag	N