DRUG FACTS

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

IODINE PREP PAD ANTISEPTIC
povidone-iodine solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:72459-017
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4)	IODINE	100 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
.BETA.-D-GLUCOPYRANOSE (UNII: J4R00M814D)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
NONOXYNOL-10 (UNII: K7O76887AP)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
POTASSIUM IODIDE (UNII: 1C4QK22F9J)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72459-017-01	0.55 g in 1 POUCH; Type 0: Not a Combination Product	02/01/2024

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M003	02/01/2024

Labeler - Yiwu Ori-Power Medtech Co.,Ltd. (560451976)

Iodine Prep Pad Antiseptic Povidone-Iodine