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Product NDC Code | 28691-0400 | ||||
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Drug Name | Wart remover |
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Type | Brand | ||||
Active Ingredients |
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Route | TOPICAL | ||||
Dosage Form | PLASTER | ||||
RxCUI drug identifier | 240559 | ||||
Application Number | part358B | ||||
Labeler Name | Pharmaplast SAE | ||||
Packages |
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Active ingredient
A list of the active, medicinal ingredients in the drug product.Active ingredient Salicylic acid 40% in a plaster vehicle
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 removal of Common and Plantar warts: Wash affected area. May soak wart in warm water for 5 minutes. Dry area thoroughly. Cut plaster to fit wart. Apply medicated plaster. Repeat procedure every 48 hours as needed (until wart is removed) for up to 12 weeks.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive ingredient Pressure sensitive adhesive fabric
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.Indications: For the removal of common warts. The common wart is easily recognized by the rough 'cauliflower-like' appearance of the surface. For the removal of plantar warts on the bottom of the foot. The plantar wart is recognized by its location only on the bottom of the foot, its tenderness, and the interruption of the footprint pattern.
Purpose
Information about the drug product’s indications for use.Purpose Wart remover adhesive pads
Spl product data elements
Usually a list of ingredients in a drug product.Wart Remover Salicylic Acid SALICYLIC ACID SALICYLIC ACID NATURAL LATEX RUBBER SILICON DIOXIDE POLYISOBUTYLENE (75000 MW) PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE)
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.Packaging 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
CURE-AID ® Pharmaplast Amria – Alexandria Egypt www.Pharmaplast-online.com
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.
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 Do not use this product on irritated skin, on any area that is infected or reddened, if you are a diabetic, or if you have poor blood circulation. If discomfort persists, see your doctor. Do not use on moles, birthmarks, warts with hair growing from them, genital warts, or warts on the face or mucous membranes. Keep out of reach of children.
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