Active Ingredient
Povidone Iodine USP 10%
Everlit Care Products Iodine Prep Pad Cloth
FDA Label NDC 83807-012
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Everlit Global Inc. for the product Everlit Care Products Iodine Prep Pad (NDC 83807-012). 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, keep out of reach of children, other information, inactive ingredients, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic for wound disinfection
Uses
Topical antimicrobial agent for wound disinfection
Warnings
Avoid contact with eyes. If happens, rinse thoroughly with water
For External Use Only.
If pain, redness, swelling, or infection develops, discontinue use and consult a phsician
Keep Out Of Reach Of Children
In case of accidental swallowing, seek medical help and contact a Poison Control Center immediately
Other Information
Store at room temperature
Inactive Ingredients
Citric acid, Alkyl Glucoside, Hydroxyethyl cellulose, Nonoxynol-9, Glycerin, Soidium hydroxide, Potassium iodine, Purified water
Directions
Tear open the packet, use iodine saturated pad to cleanse desired skin area. Discard pad appropriately after use.
* Please review the disclaimer below.
