povidine iodine

Swab · Topical

Over the counter

Active ingredient

Section Text Active Ingredient Purpose Povidone Iodine 10% w/v (9.85% w/w/) Antiseptic

Purpose

Purpose: Purpose: First aid antiseptic to help prevent skin infection in minor cuts, scrapes and burns. For preparation of the skin prior to surgery. Helps reduce bacteria that can potentially cause skin infections.

Uses

For use as an first aid antiseptic pre-operative skin preperation

Warnings

Warnings: Section Text FOR EXTERNAL USE ONLY

Do not use

Do not use: As a first aid antiseptic for more than 1 week. In the eyes. Over large areas of the body.

Ask a doctor before use

Ask a doctor before use if you have: Deep puncture wounds Animal bites Serious burns

Stop use and ask a doctor

Stop Use: If irritation and redness develop If condition persists for more than 72 hours, consult a physician.

Keep out of reach of children

Keep Out Of Reach Of Children Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center.

Directions

Directions Povidone iodine: Tear at notch, remove applicator, use only once. As a first aid antiseptic clean affected area apply 1 to 3 times daily may be covered with a sterile bandage, if bandaged let dry. For preoperative patient skin preparation clean area apply to operative site prior to surgery using the applicator

Inactive ingredients

Inactive Ingredients Inactive ingredients: Citric acid, glycerin, polysorbate 80, sodium citrate USP, sodium phosphate dibasic, water

Label text from the FDA structured product label by Dynarex Corporation (revised Mar 23, 2026). Long sections are shortened; the complete label is on DailyMed.

Active ingredients

povidine iodine NDC products (1)

NDCStrength & formLabelerType
67777-419Povidone-iodine 10 mg/mL
Swab
Dynarex CorporationOTC MONOGRAPH DRUG

Frequently asked questions

What is povidine iodine used for?

For use as an first aid antiseptic pre-operative skin preperation

Who makes povidine iodine?

povidine iodine is listed by 1 labeler in the FDA NDC directory, including Dynarex Corporation.