Povidone Iodine Pad Liquid
FDA Label NDC 59050-705
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Changzhou Maokang Medical Products Co., Ltd for the product Povidone Iodine Pad (NDC 59050-705). 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 ingredient, purpose, use, warnings, do not use, ask a doctor before use, • keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Povidone-Iodine 10%w/w
Purpose
Antiseptic
Use
For preparation of the skin prior to surgery
Warnings
For external use only.
Do not apply to persons allergic to iodine.
Do Not Use
in the eyes.
Ask A Doctor Before Use
if injuries are deep wounds, puncture wound, serious burns.
• Keep Out Of Reach Of Children.
- If swallowed or gets in eyes, get medical help, or contact a Poison Control Center right away.
Directions
Clean area. Apply to the operative site prior to surgery.
Other Information
1% titratable iodine. Store at ambient temperatures.
Inactive Ingredients
Hydroxyethyl cellulose, nonoxynol-10, alkyl glucoside, potassium iodide, sodium hydroxide, glycerin, citric acid, purified water
Package Labelling;
Label.jpg (Label)
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