POVIDONE-IODINE SCRUB STERILE- povidone-iodine swab

Povidone-Iodine Scrub Sterile by

Drug Labeling and Warnings

Povidone-Iodine Scrub Sterile by is a Otc medication manufactured, distributed, or labeled by Cardinal Health 200, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Povidone-Iodine 7.5%

Purpose

Antiseptic

Use

For preparation prior to surgery Helps to reduce bacteria that can potentially cause skin infection

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 wounds serious burns

Stop use and ask a doctor if

irritation and redness develop condition persists for more than 72 hours infection occurs

Avoid pooling beneath the patient.

Prolonged exposure to wet solution may cause skin irritation.

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 the area. Apply product to the operative site prior to surgery using sponge sticks to prep desired area.

Other information

saturating solution contains 0.75% titratable iodine latex free for hospital or professional use only

Inactive ingredients

Citric Acid, Alkyl Glucoside, Nonoxynol-10, Glycerin, Sodium Hydroxide, Potassium Iodide, Purified Water

Product Label

INGREDIENTS AND APPEARANCE

POVIDONE-IODINE SCRUB STERILE 
povidone-iodine swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63517-255
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4)	IODINE	75 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
NONOXYNOL-10 (UNII: K7O76887AP)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
POTASSIUM IODIDE (UNII: 1C4QK22F9J)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63517-255-21	25 in 1 BOX	04/29/2015
1		3 in 1 POUCH
1		4.5 g in 1 PATCH; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/29/2015

Labeler - Cardinal Health 200, Inc (961027315)