Povidone Iodine Impregnated
Povidone Iodine Impregnated is an FDA drug label for the active ingredient POVIDONE IODINE manufactured by Jianerkang Medical Co., Ltd administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231023.
Generic: POVIDONE IODINE
Manufacturer: Jianerkang Medical Co., Ltd
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 34645-4010
Application: M005
Effective: 20231023
Active Ingredients: Active Ingredients Povidone Iodine, USP 10% (1.0% available Iodine)
Indications & Usage
Uses For preparation of skin and mucous membranes prior to surgery
Dosage & Administration
Directions open pouch at tear notch use sponge sticks to prep desired area
Contraindications
Not available.
Warnings
Warnings For external use only Avoid use on persons allergic to iodine
Adverse Reactions
Not available.
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