NDC 69282-001 Nioxin Hair Regrowth Treatment For Women

Minoxidil

NDC Product Code 69282-001

NDC 69282-001-18

Package Description: 3 BOTTLE, DROPPER in 1 CARTON > 60 mL in 1 BOTTLE, DROPPER

NDC 69282-001-60

Package Description: 1 BOTTLE, DROPPER in 1 CARTON > 60 mL in 1 BOTTLE, DROPPER

NDC Product Information

Nioxin Hair Regrowth Treatment For Women with NDC 69282-001 is a a human over the counter drug product labeled by The Wella Corporation. The generic name of Nioxin Hair Regrowth Treatment For Women is minoxidil. The product's dosage form is solution and is administered via topical form. The RxNorm Crosswalk for this NDC code indicates multiple RxCUI concepts are associated to this product: 1593607 and 311723.

Dosage Form: Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Nioxin Hair Regrowth Treatment For Women Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.


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)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: The Wella Corporation
Labeler Code: 69282
FDA Application Number: ANDA075357 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: ANDA - A product marketed under an approved Abbreviated New Drug Application. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 11-01-2014 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: 12-31-2021 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: N - NO 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".

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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.

Nioxin Hair Regrowth Treatment For Women Product Label Images

Nioxin Hair Regrowth Treatment For Women 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

Other

Drug Facts

Dist. by THE WELLA CORPORATION,WOODLAND HILLS, CA 91367

Active Ingredient

Minoxidil 2% w/v

Purpose

Hair regrowth treatment

Use

To regrow hair on the scalp

Warnings

For external use onlyFlammable: 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 children.your scalp is red, inflamed, infected, irritated, or painfulyou use other medicines on the scalp

Otc - Ask Doctor

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 water.some 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 results.the 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

Otc - Pregnancy Or Breast Feeding

May be harmful if used when pregnant or breast-feeding.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

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 your hair regrowth, or hair loss will begin again

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 information.in clinical studies of mostly white women aged 18-45 years with mild to moderate degrees of hair loss, the following response to minoxidil topical solution 2% was reported: 19% of women reported moderate hair regrowth after using minoxidil topical solution 2% for 8 months (19% had moderate regrowth; 40% had minimal regrowth). This compares with 7% of women reporting moderate hair regrowth after using the placebo, the liquid without minoxidil in it, for 8 months (7% had moderate regrowth; 33% had minimal regrowth).store at 20° to 25°C (68° to 77°F). Keep tightly closed.

Inactive Ingredients

Alcohol, propylene glycol, purified water

Questions?

Call 1-800-719-9260

* Please review the disclaimer below.