Other
Freskaro Decolorized Iodine
Drug Facts
Freskaro Decolorized Iodine Liquid
FDA Label NDC 82645-207
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Pharma Nobis, Llc for the product Freskaro Decolorized Iodine (NDC 82645-207). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding other, active ingredient, purpose, uses, warnings, when using the product, stop use and consult a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Alcohol 48%
Purpose
First Aid Antiseptic
Uses
First Aid Antiseptic to help prevent infection in in minor, cuts, scrapes and burns.
Warnings
For External Use Only
When Using The Product
Do not use in the eyes or apply over large areas of the bosy. In case of deep or puncture wounds, animal bites or serious burns, consult a doctor.
Stop Use And Consult A 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 immediately. Soap will deactivate the effects of this product.
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 Ingredient
Ammonia Hydroxide, Iodine, Potassium Iodide, Purified water.
Other Information
Flammable: Keep away from spark, heat and flame
* Please review the disclaimer below.
