Otc - Active Ingredient
Active Ingredient: Povidone-Iodine USP (7.5%)
Lights Povindone Iodine Scrub Solution
FDA Label NDC 61333-205
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Lights Medical Manufacture Co., Ltd. for the product Lights Povindone Iodine Scrub (NDC 61333-205). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - ask doctor, otc - keep out of reach of children, dosage & administration, other safety information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose: Antiseptic
Indications & Usage
Use:
Antiseptic skin preparation
Warnings
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.
Otc - Ask Doctor
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
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. In case of a accidental ingestion,, seek professional assistance or consult a poison control center immediately
Dosage & Administration
Directions:
Apply locally as needed.
Other Safety Information
Other information
- Store at room temperature
- 0.75% available iodine
- Latax free
- For hospital or professional use only
Inactive Ingredient
Inactive Ingredient
Citric acid, purified water, Disodium hydrogen phosphate
* Please review the disclaimer below.
