Dosage & Administration
Clean the affected area, apply a small amount on the area 1 to 3 times daily. May be covered with a sterile bandage. If bandaged, let dry first.
Iodo Albo Iodide
FDA Label NDC 53145-120
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Menper Distributors Inc. for the product Iodo Albo Iodide (NDC 53145-120). 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 dosage & administration, otc - active ingredient, indications & usage, warnings, otc - keep out of reach of children, inactive ingredient, otc - purpose, iodo albo iodide, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
Ethyl Alcohol 48%
Indications & Usage
First aid antiseptic to help prevent skin 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.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately. Soap will deactivate the effects of this product.
Inactive Ingredient
- Ammonium Hydroxide
- Iodine
- Potassium Iodide
- Purified Water
Otc - Purpose
First Aid Antiseptic
* Please review the disclaimer below.
