APLICARE- povidone iodine swab

Aplicare by

Drug Labeling and Warnings

Aplicare by is a Otc medication manufactured, distributed, or labeled by Aplicare Products LLC, Medline Industries, LP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Povidone-iodine USP 10% w/w

Purpose

Antiseptic

Uses

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

Warnings

Do not use

• if allergic to iodine
• in the eyes
• or apply over large areas of the body
• longer than 1 week unless directed by a doctor

For external use only

Stop use and ask a doctor if

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

Avoid pooling beneath patient

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or consult a poison control center immediately.

Directions

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

Other information

• 1% titratable iodine
• not made with natural rubber latex
• for hospital or professional use only
• for single use only
• protect from freezing, avoid excessive heat

Inactive ingredients

citric acid, disodium phosphate, purified water

Manufacturer information

www.medline.com ©2024 Medline Industries, LP
Aplicare is a registered trademark of Medline Industries, LP.
Manufactured for Medline Industries, LP, Three Lakes Drive,
Northfield, IL 60093 USA. Made in China. 1-800-MEDLINE.
V1 RI24LPD

Package label

INGREDIENTS AND APPEARANCE

APLICARE 
povidone iodine swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52380-0946
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 g

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52380-0946-3	3 in 1 PACKET	09/27/2024
1		2 g in 1 APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	09/27/2024

Labeler - Aplicare Products LLC (081054904)

Registrant - Medline Industries, LP (025460908)