Active Ingredient
POVIDONE-IODINE 10% W/v (equivalent to iodine 1%)
Povidone-iodine Prep Pad
FDA Label NDC 58488-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Tongzhou Ruihong Medical Products Factory for the product Povidone-iodine Prep Pad (NDC 58488-003). 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, warnings, keep out of reach of children, directions, other information, use, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Warnings
For External use only.
Discontinue use if irritation and redness develop
Keep Out Of Reach Of Children
Keep out of reach of children
Directions
Apple locally as needed.
Other Information
Store at room temperature:59o-86oF(15--30℃)
Use
Antiseptic for preparation of the skin
Inactive Ingredients
Purified Water
Package Label.Principal Display Panel
3 (003)
* Please review the disclaimer below.
