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Dandruff - Medication Information

Product NDC Code 41250-816
Drug Name

Dandruff

Type Brand
Active Ingredients
Selenium sulfide 10 mg/ml
Route TOPICAL
Dosage Form SHAMPOO
RxCUI drug identifier 204642
Application Number M032
Labeler Name Meijer Distribution
Packages
Package NDC Code Description
41250-816-15 420 ml in 1 bottle, plastic (41250-816-15)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Selenium sulfide 1%

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 if used on bleached, gray, tinted or permed hair, rinse for at least 5 minutes

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients water, ammonium laureth sulfate, ammonium lauryl sulfate, glycol distearate, cocamide MEA, ammonium xylenesulfonate, sodium citrate, fragrance, amodimethicone, cetyl alcohol, sodium chloride, citric acid, sodium benzoate, stearyl alcohol, disodium EDTA, hydrogen peroxide, hydroxypropyl methylcellulose, methylchlorisothiazolinone, methylisothiazolinone, red 4

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 itching, irritation, redness, flaking and scaling associated with dandruff and seborrheic dermatitis

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Dandruff Selenium sulfide WATER AMMONIUM LAURETH-3 SULFATE AMMONIUM LAURYL SULFATE GLYCOL DISTEARATE COCO MONOETHANOLAMIDE AMMONIUM XYLENESULFONATE SODIUM CITRATE AMODIMETHICONE (800 CST) CETYL ALCOHOL SODIUM CHLORIDE CITRIC ACID MONOHYDRATE SODIUM BENZOATE STEARYL ALCOHOL EDETATE DISODIUM HYDROGEN PEROXIDE HYPROMELLOSES METHYLCHLOROISOTHIAZOLINONE METHYLISOTHIAZOLINONE FD&C RED NO. 4 SELENIUM SULFIDE SELENIUM SULFIDE

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.
principal display panel Meijer Advanced Solution dandruff shampoo dandruff and seborrheic dermatitis shampoo with selenium sulfide Maximum Strength helps relieve even stubborn dandruff COMPARE TO THE ACTIVE INGREDIENT OF HEAD & SHOULDERS CLINICAL STRENGTH* 14.2 FL OZ (420mL) image description

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Helps fight dandruff from the 1st wash. Contains 1% selenium sulfide to help reduct the symptoms of dandruff and seborrheic dermatitis: itching, Flaking, Scaling, irritation and redness. *This product is not manufactured or distributed by Procter + Gamble, distributor of Head + Shoulders Clinical Strength Dandruff Shampoo DIST. BY MEIJER DISTRIUBTION, INC. 2929 WALKER AVE NW GRAND RAPIDS, MI 49544 www.meijer.com

Ask doctor

Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.
Ask a doctor before use if condition covers a large area of the body

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 Poison 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

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product do not get into eyes. If contact occurs, rinse eyes thoroughly with water.

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

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