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Lights povindone iodine scrub - Medication Information

Product NDC Code 61333-205
Drug Name

Lights povindone iodine scrub

Type Brand
Active Ingredients
Povidone-iodine .75 g/100g
Route TOPICAL
Dosage Form SOLUTION
RxCUI drug identifier 314188
Application Number M003
Labeler Name Lights Medical Manufacture Co., Ltd.
Packages
Package NDC Code Description
61333-205-01 118 g in 1 bottle (61333-205-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient: Povidone-Iodine USP (7.5%)

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 needed.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredient Citric acid, purified water, Disodium hydrogen phosphate

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 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.
Lights Povindone Iodine Scrub POVIDONE-IODINE CITRIC ACID MONOHYDRATE WATER SODIUM PHOSPHATE DIBASIC DIHYDRATE 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 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 or puncture wounds Serious burns Stop use and ask a doctor if Redness, irritation, swelling or pain persisits or increases Infection occurs

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 a 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 Store at room temperature 0.75% available iodine Latax free 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: Do not use if allergic to iodine For external use only Do not use in eyes Avoid pooling beneath patient. Prolonged exposure to wet solution may cause skiin irritation.

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