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Product NDC Code | 34645-4050 | ||||
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Drug Name | Povidone iodine scrub |
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Type | Brand | ||||
Active Ingredients |
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Route | TOPICAL | ||||
Dosage Form | SWAB | ||||
RxCUI drug identifier | 797730 | ||||
Application Number | M005 | ||||
Labeler Name | Jianerkang Medical Co., Ltd | ||||
Packages |
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Active ingredient
A list of the active, medicinal ingredients in the drug product.Active Ingredient Povidone Iodine USP, 10% W/V (equivalent to 1% titratable iodine)
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 preparation of the skin prior to surgery clean the affected area, remove swab by stick apply to the operative site prior to surgery clean the affected area apply a small amount of this products on the area 1-3 times daily may be covered with a sterile bandage if bandaged, let dry first For use as a first aid antiseptic
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive ingredients citric acid, purified water, sodium hydroxide, Nonoxynol-10, glycerin
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.Health-care antiseptic for preparation of the skin prior to surgery First aid antiseptic to help prevent the risk of skin infection in minor cuts, scrapes, and burns Use
Purpose
Information about the drug product’s indications for use.Purpose Antiseptic
Spl product data elements
Usually a list of ingredients in a drug product.Povidone Iodine Scrub Povidone-Iodine CITRIC ACID MONOHYDRATE WATER SODIUM HYDROXIDE NONOXYNOL-10 GLYCERIN POVIDONE-IODINE IODINE
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.Image of Pouch Label Pouch Label
Do not use
Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.use in the eyes use on individuals who are allergic or sensitive to iodine apply over larger areas of the body use as a first aid antiseptic longer than 1 week unless by a doctor Do not
if irritation and redness develop, consult a doctor in case of deep or puncture wounds animal bites serious burns Discontinue use
Stop use and consult a doctor if the condition persists or gets worse
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.If swallowed, get medical help or contact a Poison Control Center right away Keep out of reach of children
Storage and handling
Information about safe storage and handling of the drug product.Other information store at room temperature: 15o - 30oC (59o-86oF)
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