POVIDONE IODINE SWABSTICKS 4 TRIPLE- povidone-iodine swab

Povidone Iodine Swabsticks 4 Triple by

Drug Labeling and Warnings

Povidone Iodine Swabsticks 4 Triple by is a Otc medication manufactured, distributed, or labeled by Amsino healthcare (USA) inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Povidone-lodine USP10%

Purpose

Antiseptic

Use

for antiseptic skin preparation

Warnings

• do not use if allergic to iodine
• do not use in the eyes

Stop use and ask a doctor if

• redness,irritation,swelling or pain persists or increases
• infection occurs

Keep out of reach of children.

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

Avoid pooling beneath patient.

Ask a doctor before use if

injuries are

For external use only.

• deep or puncture wounds
• serious burns

Directions

apply locally as needed

Other information

• 1% titratable iodine
• For hospital or professional use only
• Store at room temperature.
• Avoid excessive heat.
• Not made with natural rubber latex.

Inactive ingredients:

Citric Acid,Alkyl Glucoside,Hydroxyethyl Cellulose,Nonoxynol-10,Glycerin,Sodium Hydroxide,Potassium lodide,Purified Water.

Package Labeling:

INGREDIENTS AND APPEARANCE

POVIDONE IODINE SWABSTICKS 4 TRIPLE 
povidone-iodine swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72838-0360
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
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: 72838-0360-1	3 in 1 POUCH	01/30/2022
1		2 g in 1 APPLICATOR; 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 Drug	505G(a)(3)	01/30/2022

Labeler - Amsino healthcare (USA) inc. (116914622)