CVS POVIDONE IODINE- povidone iodine swab

CVS Povidone Iodine by

Drug Labeling and Warnings

CVS Povidone Iodine by is a Otc medication manufactured, distributed, or labeled by CVS Pharmacy Inc, Medline Industries, LP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Povidone-Iodine 10% w/v

Purpose

First aid antiseptic

Uses

• first aid antiseptic to help prevent infection in minor cuts, scrapes and burns

Warnings

For external use only.

Do not use

• in the eyes
• longer than one week unless directed by a physician
• on individuals who are allergic or sensitive to iodine
• over large areas of the body

Stop use and ask a doctor

• irritation and redness develop
• condition persists for more than 72 hours
• in case of deep or puncture wounds, animal bites or serious burns

Keep out of reach of children.

If swallowed, seek medical assistance or immediately contact a Poison Control Center.

Directions

• clean the affected area
• apply a small amount of this product on the area 1-3 times daily
• may be covered with a sterile bandage
• if bandaged, let dry first

Other information

• protect from freezing and avoid excessive heat

Inactive ingredients

citric acid, disodium phosphate, purified water

Manufacturing Information

Distributed by:

CVS Pharmacy, Inc.

One CVS Drive, Woonsocket, RI 02895 USA

Made in China

www.CVS.com

1-800-SHOP CVS

REF: CVS239100

V2 RK21LPD

Package Label

INGREDIENTS AND APPEARANCE

CVS POVIDONE IODINE 
povidone iodine swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-935
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4)	IODINE	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-935-10	10 in 1 BOX	09/01/2020
1		6 mL in 1 POUCH; Type 0: Not a Combination Product
2	NDC: 69842-935-01	6 mL in 1 POUCH; Type 0: Not a Combination Product	09/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	09/01/2020

Labeler - CVS Pharmacy Inc (062312574)

Registrant - Medline Industries, LP (025460908)