Decolorized Iodine
Decolorized Iodine is an FDA drug label for the active ingredient ETHYL 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 20231222.
Generic: ETHYL ALCOHOL
Manufacturer: Pharma Nobis, LLC
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 82645-909
Application: M003
Effective: 20231222
Active Ingredients: Active Ingredients Alcohol 45 % denatured with ammonia, Ammonium and Potassium Iodides.
Indications & Usage
Uses First aid to help prevent infection in minor cuts, scrapes and burns.
Dosage & Administration
Directions Clean the affected area. Aply a small amount to the affected area 1 to 3 times daily. May be covered with a sterile bandage. If bandaged, let it dry first.
Contraindications
Not available.
Warnings
Warnings For external use only.
Adverse Reactions
Not available.
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