Active Ingredient
POVIDONE-IODINE USP 10%
Povidone-iodine Solution
FDA Label NDC 58488-006
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 Solution (NDC 58488-006). 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
Do not use if allergic to iodine.
For External use only.
Ask a doctor before use if injuries are
--Deep or puncture wounds
--serious bums
stop use ask a doctor if
--reness ,irritation ,swelling or pain persists or increases
--infection occurs
Do not use in eyes
Avoid "pooling "benesth patient.Prolonged exposure to wet solution may cause skin irrtation.
Keep Out Of Reach Of Children.
Keep out of reach of children.in case of axxidental ingestion,seek professional assistance or consult a poison control center immediately.
Directions
Apple locally as needed.
Other Information
--1% titrarabil iodine --latex free ---for hospital or professional use only
Use
Antiseptic skin preparation
Inactive Ingredients
citric acid,disodium,phosphate,nonoxynol-9,sodium hydrexide,Water
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Label (Label)
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