Sunmark Iodine
Iodine, Sodium Iodide, Alcohol · Tincture · Topical
Active ingredient
Active Ingredients Iodine 2%, Sodium Iodide 2.4%, Alcohol 47%
Purpose
Purpose Antiseptic
Uses
Uses To help prevent infection in minor cuts, scrapes and burns.
Warnings
WARNINGS: For external use only.
Keep out of reach of children
In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.
Directions
DIRECTIONS: Clean the affected area. Apply a small amount to the affected area 1 to 3 times daily. May be covered with a sterile bandage. If bandaged, let dry first.
Inactive ingredients
Inactive ingredient: Purified Water.
Label text from the FDA structured product label by Strategic Sourcing Services LLC (revised Dec 19, 2023). Long sections are shortened; the complete label is on DailyMed.
Active ingredients
- Iodine in 1 product
- Alcohol in 1 product
- Sodium Iodide in 1 product
Sunmark Iodine NDC products (1)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 49348-133 | Iodine 20 mg/mL; Alcohol 470 mg/mL; Sodium Iodide 24 mg/mL Tincture | Strategic Sourcing Services LLC | OTC MONOGRAPH DRUG |
Frequently asked questions
What is Sunmark Iodine used for?
Uses To help prevent infection in minor cuts, scrapes and burns.
Who makes Sunmark Iodine?
Sunmark Iodine is listed by 1 labeler in the FDA NDC directory, including Strategic Sourcing Services LLC.