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Tm titus medical povidone iodine - Medication Information

Product NDC Code 81526-002
Drug Name

Tm titus medical povidone iodine

Type Brand
Active Ingredients
Povidone-iodine 1 g/100g
Route TOPICAL
Dosage Form OINTMENT
RxCUI drug identifier 312563
Application Number M003
Labeler Name Titus Medical LLC
Packages
Package NDC Code Description
81526-002-01 100 pouch in 1 box (81526-002-01) / 1 g in 1 pouch
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Povidone-Iodine USP (10%)

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 Apply locally as need

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredient Glycerin, Propylene Glycol, PEG 1450, Sodium Hydrogen Phosphate, Citric Acid, 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 Antiseptic skin preparation

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.
TM Titus Medical Povidone Iodine POVIDONE-IODINE PROPYLENE GLYCOL POVIDONE-IODINE IODINE WATER CITRIC ACID MONOHYDRATE SODIUM PHOSPHATE, DIBASIC GLYCERIN

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 description image description

Ask doctor

Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.
Ask a doctor before use if injuries are deep wounds, puncture wounds or serious burns Stop use and ask a doctor if infection occurs or if redness, irritation, swelling, or pain persists or increases

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. In case of accidental ingestion, seek professional assistance or consult a poison control center immediately

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
Other information not made with natural rubber latex for hospital or professional use only

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 if allergic to iodine in the eyes

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