Freskaro Decolorized Iodine
Freskaro Decolorized Iodine is an FDA drug label for the active ingredient ALCOHOL manufactured by Pharma Nobis, LLC administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231228.
Generic: ALCOHOL
Manufacturer: Pharma Nobis, LLC
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 82645-207
Application: M003
Effective: 20231228
Active Ingredients: Active Ingredient Alcohol 48%
Indications & Usage
Uses First Aid Antiseptic to help prevent infection in in minor, cuts, scrapes and burns.
Dosage & Administration
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.
Contraindications
Not available.
Warnings
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.
Adverse Reactions
Not available.
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