NDC 0363-2173 Solution

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  2. Walgreens
  3. NDC: 0363-2173 Solution

NDC Product Code 0363-2173

NDC CODE: 0363-2173

Proprietary Name: Solution What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

NDC Code Structure

NDC 0363-2173-02

Package Description: 1 BOTTLE in 1 PACKAGE > 60 mL in 1 BOTTLE

NDC 0363-2173-05

Package Description: 3 BOTTLE in 1 PACKAGE > 60 mL in 1 BOTTLE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Solution with NDC 0363-2173 is a product labeled by Walgreens. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 311723.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.
  • ALCOHOL (UNII: 3K9958V90M)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Walgreens
Labeler Code: 0363
Start Marketing Date: 08-08-2014 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2019 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.
Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Information for Patients

Minoxidil Oral

Minoxidil Oral is pronounced as (mi nox' i dill)

Why is minoxidil oral medication prescribed?
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...
[Read More]
Minoxidil Topical

Minoxidil Topical is pronounced as (mi nox' i dill)
Why is minoxidil topical medication prescribed?
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 o...
[Read More]

* Please review the disclaimer below.

Solution Product Label Images

Solution Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

Minoxidil 2% w/v..........................................................................................................Hair regrowth treatment

Use

To regrow hair on the scalp (vertex only, see picture on side of carton)

Warningsfor External Use Only.

Flammable: Keep away from fire or flame

Do Not Use If:

  • Your degree of hair loss is different than that shown on the side of this carton, because this product may not work for youYou have no family history of hair lossYour hair loss is sudden and/or patchyYour hair loss is associated with childbirthYou do not know the reason for your hair lossYou are under 18 years of age. Do not use on babies and childrenYour scalp is red, inflamed, irritated or painfulYou use other medicines on the scalp

Ask A Doctor Before Use If You Have:

  • Heart Disease

When Using This Product:

  • Do not apply on other parts of the bodyAvoid contact with the eyes. In case of accidental contact, rinse eyes with large amounts of cool tap waterSome people have experienced changes in hair color and/or textureIt takes time to regrow hair. You may need to use this product 2 times a day for at least 4 months before you see resultsThe amount of hair regrowth is different for each person. This product will not work for everyone

Stop Use And Ask A Doctor If:

  • Chest pain, rapid heartbeat, faintness, or dizziness occursSudden, unexplained weight gain occursYour hands or feet swellScalp irritation or redness occursUnwanted facial hair growth occursYou do not see hair regrowth in 4 months

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

Other Information:

  • See hair loss pictures on side of this cartonBefore use, read all information on carton and enclosed leafletKeep the carton. It contains important informationIn clinical studies of mostly white women aged 18-49 years wiht mild to moderate degrees of hair loss, the following response to 2% minoxidil topical solution was reported: 19% of women reported moderate hair regrowth after using 2% minoxidil topical solution for 8 months (19% had moderate regrowth; 40% had minimal regrowth). This compares with 7% of women reporting moderate hair regrowth after using placebo, the liquid without minoxidil in it for 8 months (7% had moderate regrowth, 33% had minimal regrowth)Store at controlled room temperature 20​o​ to 25​o​C (68​o​ to 77​o​F). Keep tightly closed.

Directions:

  • Apply one mL with dropper 2 times a day directly onto the scalp in the hair loss areaUsing more or more often will not improve resultsContinued use is necessary to increase and keep you hair regrowth, or hair loss will begin again

Inactive Ingredients

Alcohol, Propylene Glycol, Purified Water

* Please review the disclaimer below.