Iodine Prep Pad Antiseptic Solution
FDA Label NDC 72459-017
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Yiwu Ori-power Medtech Co.,ltd. for the product Iodine Prep Pad Antiseptic (NDC 72459-017). 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 drug facts, active ingredients, purpose, inactive ingredients, use, directions, storage, warnings, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Povidone Iodine 10% USP.
Purpose
First aid to help reduce the risk of infection in minor cuts, scrapes, and burns.
Inactive Ingredients
Citric Acid, Glucoside, Hydroxyethyl Cellulose, Nonoxynol-10, Glycerin, Sodium Hydroxide, Potassium Iodide, Purified Water.
Use
Topical Antimicrobial Agent For Wound Disinfection.
Directions
Tear open packet, use Iodine-saturated pad to cleanse desired skin area. Discard pad appropriately after use.
Storage
Store at room temperature 15°C - 30°C (59°F - 86°F).
Warnings
Avoid contact with eyes. If happens, rinse thoroughly with water. For External Use Only. If pain, irritation, redness, swelling, or infection develops, discontinue use and consult physician.
Keep Out Of Reach Of Children
In case of accidental swallowing, seek medical help and contact poison control immediately.
Package Labeling:
Label3 (Label3)
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