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Product NDC Code | 72811-002 | ||||
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Drug Name | 111medco medicated bar 2 pyrithione zinc |
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Type | Brand | ||||
Active Ingredients |
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Route | TOPICAL | ||||
Dosage Form | SOAP | ||||
RxCUI drug identifier | 283707 | ||||
Application Number | M032 | ||||
Labeler Name | 111MedCo LLC | ||||
Packages |
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Active ingredient
A list of the active, medicinal ingredients in the drug product.Active ingredient Pyrithione Zine 2% Purpose Dandruff/Seborrheic Dermatitis
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 Use on affected areas in place of your regular soap For best results use at least twice a week or as directed by your healthcare provider
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive ingredients Sodium palmate, sodium cocoate*, sodium palm kernelate*, agua, glycerin, orange extract, sodium chloride, pentasodium pentetate. (*may contain this ingredient)
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 For relief of skin itching, flaking, and scaling associated with dandruff and seborrheic dermatitis
Purpose
Information about the drug product’s indications for use.Purpose Dandruff/Seborrheic Dermatitis
Spl product data elements
Usually a list of ingredients in a drug product.111MedCo Medicated Bar 2 Pyrithione Zinc PYRITHIONE ZINC SODIUM PALMATE SODIUM COCOATE SODIUM PALM KERNELATE WATER GLYCERIN SODIUM CHLORIDE PENTASODIUM PENTETATE PYRITHIONE ZINC PYRITHIONE ZINC
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: Label0
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
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 medial help or contact a Poison Control Center right away.
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 skin irritation and dryness may occur if you use other topical acne medications at the same time or immediately following use of this product. If this occurs, use only one medication at a time unless directed by a healthcare provider.
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 skin irritation and dryness may occur if you use other topical acne medications at the same time or immediately following use of this product. If this occurs, use only one medication at a time unless directed by a healthcare provider. Keep out of reach of children. If swallowed, get medial help or contact 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