KONIX POVIDONE IODINE TOPICAL ANTISEPTIC- povidone-iodine liquid

Konix Povidone Iodine Topical Antiseptic by

Drug Labeling and Warnings

Konix Povidone Iodine Topical Antiseptic by is a Otc medication manufactured, distributed, or labeled by TURKUAZ SAGLIK HIZMETLERI MEDIKAL TEMIZLIK KIMYASAL URUNLER SANAYI VE TICARET AS. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Povidone-iodine 7.5%

Purpose

Antiseptic, First Aid Antiseptic

Uses

• For preparation of the skin prior to surgery.
• Helps reduce bacteria that potentially can cause skin infection.
• First aid to help reduce the risk of skin infection in minor cuts, scrapes, and burns.

Warnings

For external use only

Do not use

• In the eyes or apply over large areas of the body. In case of deep or puncture wounds, animal bites, or serious burns, consult a doctor.

Stop use and ask a doctor if

• condition persists or gets worse. Do not use longer than 1 week unless directed by a doctor.
• irritation and redness develop.
• if conditions persists for more than 72 hours.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away

Directions

• Patient Preperative Skin Preparation: Clean the area. Apply product to the operative site prior to sugery.
• First Aid:Clean the affected area. 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

• Protect from freezing. Avoid excessive heat. Store at room temperature
• Not made with natural rubber latex. For hospital and professional use only.

Inactive ingredients

Cellulose, 2-hydroxyethyl ether, Sodium Lauryl Ether Sualphate, Disodium Hydrogenorthophosphate, Potassium Iodide, Sodium Hydroxide, Water

Package Labeling:

INGREDIENTS AND APPEARANCE

KONIX POVIDONE IODINE TOPICAL ANTISEPTIC 
povidone-iodine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73107-008
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 mL

Inactive Ingredients
Ingredient Name	Strength
POWDERED CELLULOSE (UNII: SMD1X3XO9M)
POTASSIUM IODIDE (UNII: 1C4QK22F9J)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73107-008-01	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/18/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	08/18/2025

Labeler - TURKUAZ SAGLIK HIZMETLERI MEDIKAL TEMIZLIK KIMYASAL URUNLER SANAYI VE TICARET AS (356325295)

Registrant - TURKUAZ SAGLIK HIZMETLERI MEDIKAL TEMIZLIK KIMYASAL URUNLER SANAYI VE TICARET AS (356325295)

Establishment
Name	Address	ID/FEI	Business Operations
TURKUAZ SAGLIK HIZMETLERI MEDIKAL TEMIZLIK KIMYASAL URUNLER SANAYI VE TICARET AS		356325295	manufacture(73107-008)