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Povidone iodine - Medication Information

Product NDC Code 34645-4188
Drug Name

Povidone iodine

Type Generic
Active Ingredients
Povidone-iodine 10 mg/ml
Route TOPICAL
Dosage Form SOLUTION
RxCUI drug identifier 312564
Application Number M005
Labeler Name Jianerkang Medical Co., Ltd
Packages
Package NDC Code Description
34645-4188-6 88.5 ml in 1 bottle, plastic (34645-4188-6)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredients Povidone Iodine, USP 10% (1.0% available 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.
Other information store at room temperature avoid excessive heat (above 104oF/40oC) protect from freezing latex free

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Citric Acid, Glycerin, Nonoxynol - 10, Purified Water, Sodium hydroxide, hydroxyethylcellulose

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 Prepping intact skin and mucous membranes prior to surgery Directions Patient preoperative prep use full strength apply solution to operative site following povidone iodine scrub application using a circular motion, start at incision site and move outward remove all soiled underdrapes do not allow solution to pool

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 Povidone Iodine CITRIC ACID MONOHYDRATE GLYCERIN NONOXYNOL-10 WATER SODIUM HYDROXIDE 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.
Package Label Pouch Label

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 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 Skin shows symptoms of irritation, sensitivity, redness, pain or swelling

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 Avoid use on persons allergic to iodine

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