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Povidone-iodine prep pads medium - Medication Information

Product NDC Code 53329-941
Drug Name

Povidone-iodine prep pads medium

Type Brand
Active Ingredients
Povidone-iodine 10 mg/ml
Route TOPICAL
Dosage Form CLOTH
RxCUI drug identifier 797730
Application Number part333E
Labeler Name Medline Industries, LP
Packages
Package NDC Code Description
53329-941-09 1 ml in 1 packet (53329-941-09)
53329-941-30 100 packet in 1 box (53329-941-30) / 1 ml in 1 packet (53329-941-09)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Povidone-Iodine, 10% w/w

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 clean the affected area apply a small amount of this product on the area 1 to 3 times daily. may be covered with a sterile bandage if bandaged, let dry first

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients citric acid, disodium phosphate, water

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 First aid antiseptic to help prevent infection in minor cuts, scrapes and burns

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 Prep Pads Medium Povidone-Iodine SODIUM PHOSPHATE, DIBASIC, ANHYDROUS CITRIC ACID MONOHYDRATE WATER POVIDONE-IODINE IODINE Povidone-Iodine Prep Pads Medium Bulk Povidone-Iodine SODIUM PHOSPHATE, DIBASIC, ANHYDROUS CITRIC ACID MONOHYDRATE WATER 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.
Principal Display Panel PDP Principal Display Panel PDP2

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.
Do not use in the eyes longer than 1 week unless directed by a physician on individuals who are allergic or sensitive to iodine or apply over large areas 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 assistance or immediately contact a Poison Control Center.

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 irritation and redness develop condition persists for more than 72 hours in case of deep or puncture wounds, animal bites or serious burns

Storage and handling

Information about safe storage and handling of the drug product.
Other information do not flush protect from freezing, avoid excessive heat

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 in the eyes longer than 1 week unless directed by a physician on individuals who are allergic or sensitive to iodine or apply over large areas of the body Stop use and ask a doctor if irritation and redness develop condition persists for more than 72 hours in case of deep or puncture wounds, animal bites or serious burns Keep out of reach of children. If swallowed, get medical assistance or immediately contact a Poison Control Center.

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