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Urban wash dandruff - Medication Information

Product NDC Code 80801-101
Drug Name

Urban wash dandruff

Type Brand
Active Ingredients
Pyrithione zinc .3 g/100ml
Route TOPICAL
Dosage Form SHAMPOO
RxCUI drug identifier 1052932
Application Number M032
Labeler Name Primal Elements
Packages
Package NDC Code Description
80801-101-01 355 ml in 1 bottle, plastic (80801-101-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Pyrithione zinc 0.3%

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions • shake well • for maximum dandruff control, use every time you shampoo • wet hair, massage onto scalp, rinse, repeat if desired • for best results, use at least twice a week or as directed by a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Water (Aqua), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Lauryl Sulfate, Cocamide MEA, Styrene/Acrylates Copolymer, Guar Hydroxypropyltrimonium Chloride, Sodium Citrate, Fragrance, Sodium Chloride, Dimethicone, Methylisothiazolinone, Iodopropynyl Butylcarbamate

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Use helps prevent recurrence of flaking and itching associated with dandruff.

Purpose

Information about the drug product’s indications for use.
Purpose Anti-dandruff

Spl product data elements

Usually a list of ingredients in a drug product.
URBAN WASH DANDRUFF pyrithione zinc SODIUM CITRATE SODIUM CHLORIDE METHYLISOTHIAZOLINONE DIMETHICONE IODOPROPYNYL BUTYLCARBAMATE FD&C BLUE NO. 1 WATER SODIUM LAURETH SULFATE PYRITHIONE ZINC PYRITHIONE ZINC COCAMIDOPROPYL BETAINE SODIUM LAURYL SULFATE GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE)

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
label

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children. If swallowed, get medical help or contact a Posion Control Center right away.

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop use and ask a doctor if condition worsens or does not improve after regular use as directed.

Storage and handling

Information about safe storage and handling of the drug product.
Other information Store at room temperature.

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings For external use only. When using this product do not get into eyes. If contact occurs, rinse eyes thoroughly with water.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API