Tm Titus Medical Povidone Iodine Ointment
FDA Label NDC 81526-002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Titus Medical Llc for the product Tm Titus Medical Povidone Iodine (NDC 81526-002). 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 ingredient, purpose, uses, warnings, otc - keep out of reach of children, otc - ask doctor, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Povidone-Iodine USP (10%)

Purpose

Antiseptic

Uses

Antiseptic skin preparation

Warnings

For external use only

Do not use if allergic to iodine in the eyes

Otc - Keep Out Of Reach Of Children

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

Otc - Ask Doctor

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

Directions

Apply locally as need

Other Information

  • not made with natural rubber latex
  • for hospital or professional use only

Inactive Ingredient

Glycerin, Propylene Glycol, PEG 1450, Sodium Hydrogen Phosphate, Citric Acid, Water

Package Label.Principal Display Panel

Image Description (0621 1)

Image Description (0621 1)

Image Description (0621 2)

Image Description (0621 2)

* Please review the disclaimer below.