Top Care Decolorized Iodine Liquid
FDA Label NDC 36800-207

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Topco Associates Llc for the product Top Care Decolorized Iodine (NDC 36800-207). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredients, purpose, uses, warnings, ask a doctor before use if you have, stop use and ask a doctor if:, when using this product:, keep out of the reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

Alcohol 45 % denatured with ammonia, Ammonium and Potassium Iodides.

Purpose

Antiseptic

Uses

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

Warnings

For external use only.

Ask A Doctor Before Use If You Have

deep or puncture wounds, animal bites, serious burns.

Stop Use And Ask A Doctor If:

The condition persists or gets worse, or if using this product for longer than 1 week.

When Using This Product:

Do not use in the eyes. If contact occurs, flush with large amounts of water while lifting upper and lower lids. Do not apply over large areas of the body.

Keep Out Of The Reach Of Children.

In case of acidental ingestion give milk, then give a starch solution made by mixing two tablespoonfools of cornstarch or flour to a pint of water. contact a poison Control Center immediately.

Directions

Clean the affected area. Aply a small amount to the affected area 1 to 3 times daily. May be covered with a sterile bandage. If bandaged, let it dry first.

Inactive Ingredient:

Purified Water

Pther Information:

Will stain skin and clothing

* Please review the disclaimer below.