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Sulfur 8 medicated dandruff with salicylic acid - Medication Information

Product NDC Code 12022-039
Drug Name

Sulfur 8 medicated dandruff with salicylic acid

Type Brand
Active Ingredients
Salicylic acid 20 mg/ml
Route TOPICAL
Dosage Form LIQUID
RxCUI drug identifier 205104
Application Number M032
Labeler Name J. Strickland and Co.
Packages
Package NDC Code Description
12022-039-00 222 ml in 1 bottle (12022-039-00)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Salicylic Acid, 2% Purpose Antidandruff, Seborrheic dermatitis, Psoriasis.

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 For best results, use at least twice a week or as directed by a doctor. Apply a liberal amount of shampoo and massage into lather. Allow lather to remain on scalp for a few minutes. Rinse and repeat.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingrdients Water, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Sodium Chloride, Polyquaternium-22, Menthol, Aloe Barbadensis Leaf Extract, PEG-40 Hydrogenated Castor Oil, Phenoxyethanol, Caprylyl Glycol, Ethylhexylglycerin, Disodium EDTA, Sodium Benzoate, Citric Acid, Potassium Sorbate, Sodium Sulfite, Sodium Hydroxide, Benzyl Benzoate, Fragrance.

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.
Uses control the symptoms of dandruff seborrheic dermatitis psoriasis

Purpose

Information about the drug product’s indications for use.
Purpose Antidandruff, Seborrheic dermatitis, Psoriasis.

Spl product data elements

Usually a list of ingredients in a drug product.
Sulfur 8 Medicated Dandruff with Salicylic Acid SALICYLIC ACID WATER SODIUM C14-16 OLEFIN SULFONATE COCAMIDOPROPYL BETAINE SODIUM CHLORIDE MENTHOL ALOE VERA LEAF POLYOXYL 40 HYDROGENATED CASTOR OIL PHENOXYETHANOL CAPRYLYL GLYCOL ETHYLHEXYLGLYCERIN EDETATE DISODIUM ANHYDROUS SODIUM BENZOATE CITRIC ACID MONOHYDRATE POTASSIUM SORBATE SODIUM SULFITE SODIUM HYDROXIDE BENZYL BENZOATE SALICYLIC ACID SALICYLIC ACID

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.
Package Labeling: Label

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.
Drug Facts

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 you have a condition that 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 call 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 of this product 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 avoid contact with 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 Ask a doctor before use if you have a condition that covers a large area of the body. When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. Stop use and ask a doctor if condition worsens or does not improve after regular use of this product as directed. Keep out of reach of children. If swallowed, get medical help or call a Poison Control Center right away.

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