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Op first aid series povidone iodine prep pad - Medication Information

Product NDC Code 72459-012
Drug Name

Op first aid series povidone iodine prep pad

Type Brand
Active Ingredients
Povidone-iodine 100 mg/ml
Route TOPICAL
Dosage Form CLOTH
RxCUI drug identifier 797730
Application Number 505G(a)(3)
Labeler Name Yiwu Ori-Power Medtech Co.,Ltd.
Packages
Package NDC Code Description
72459-012-01 1 patch in 1 pouch (72459-012-01) / .55 ml in 1 patch
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredients Povidone Iodine 10% USP (equivalent to iodine 1%) Purpose Antiseptic

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 intended area thoroughly with pad.discard after single use.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Citric Acid, Alkyl Glucoside,Hydroxyethyl Cellulose, Nonoxynol-10, Glycerin, Sodium Hydroxide, Potassium Iodide, Purified 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.
Use Antiseptic for preparation of the skin. First aid antiseptic to help prevent skin infection.

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.
OP First Aid Series Povidone Iodine Prep Pad POVIDONE-IODINE CITRIC ACID MONOHYDRATE HYDROXYETHYL CELLULOSE, UNSPECIFIED NONOXYNOL-10 GLYCERIN SODIUM HYDROXIDE POTASSIUM IODIDE 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.
Package Labeling: Bottle3

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 Other information Store at room temperature 15°C-30°C (59°F-86°F).

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 Avoid contact with eyes.If happens,rinse thoroughly with water.

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 a 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 In case of deep or puncture wounds or serious burns,and if pain,irritation, redness, swelling,or infection occurs,discontinue use and contact a physician.

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 Avoid contact with eyes.If happens,rinse thoroughly with water. Stop use In case of deep or puncture wounds or serious burns,and if pain,irritation, redness, swelling,or infection occurs,discontinue use and contact a physician. Keep out of reach of children If swallowed, get medical 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