FDA Label for Sunmark Iodides Tincture
View Indications, Usage & Precautions
Sunmark Iodides Tincture Product Label
The following document was submitted to the FDA by the labeler of this product Strategic Sourcing Services Llc. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient
Ethyl Alcohol 48%
Purpose
First Aid Antiseptic
Use
first aid to help prevent infection in minor cuts, scrapes and burns.
Warnings
For external use only
When Using This Product
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 Consult Doctor If The
condition persists or gets worse. Do not use this product for longer than 1 week unless directed by a doctor.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Clean the affected area.
- apply a small amount on the area 1 to 3 times daily.
- may be covered with sterile bandage.
- if bandaged, let dry first.
Other Information
store at room temperature
Inactive Ingredients
ammonium hydroxide, iodine, potassium iodide, and purified water
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