NDC 69423-586 Head And Shoulders Scalp X Minoxidil Hair Regrowth Treatment For Women
Minoxidil Aerosol, Foam Topical - View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 69423-586?
What are the uses for Head And Shoulders Scalp X Minoxidil Hair Regrowth Treatment For Women?
What are Head And Shoulders Scalp X Minoxidil Hair Regrowth Treatment For Women Active Ingredients?
- MINOXIDIL 5 g/100g - A potent direct-acting peripheral vasodilator (VASODILATOR AGENTS) that reduces peripheral resistance and produces a fall in BLOOD PRESSURE. (From Martindale, The Extra Pharmacopoeia, 30th ed, p371)
Which are Head And Shoulders Scalp X Minoxidil Hair Regrowth Treatment For Women UNII Codes?
The UNII codes for the active ingredients in this product are:
- MINOXIDIL (UNII: 5965120SH1)
- MINOXIDIL (UNII: 5965120SH1) (Active Moiety)
Which are Head And Shoulders Scalp X Minoxidil Hair Regrowth Treatment For Women Inactive Ingredients UNII Codes?
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. The UNII codes for the inactive ingredients in this product are:
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- BUTANE (UNII: 6LV4FOR43R)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- ISOBUTANE (UNII: BXR49TP611)
- LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
- DEHYDRATED ALCOHOL (UNII: 3K9958V90M)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- PROPANE (UNII: T75W9911L6)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Head And Shoulders Scalp X Minoxidil Hair Regrowth Treatment For Women?
- RxCUI: 2584341 - Head & Shoulders Scalp X 5 % Topical Foam
- RxCUI: 2584341 - minoxidil 50 MG/ML Topical Foam [Head & Shoulders Scalp X]
- RxCUI: 2584341 - Head & Shoulders Scalp X 50 MG/ML Topical Foam
- RxCUI: 645146 - minoxidil 5 % Topical Foam
- RxCUI: 645146 - minoxidil 50 MG/ML Topical Foam
Which are the Pharmacologic Classes for Head And Shoulders Scalp X Minoxidil Hair Regrowth Treatment For Women?
* Please review the disclaimer below.
Patient Education
Minoxidil
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.
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Minoxidil Topical
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.
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* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] 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.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] 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.
[8] 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.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
[12] 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".