Inofoam Antibacterial Foaming Hand Wash Liquid
FDA Label NDC 73062-032
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Avro Enterprises, Llc for the product Inofoam Antibacterial Foaming Hand Wash (NDC 73062-032). 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 drug facts, active ingredient, purppose, uses, warings, when using this product, stop use and ask 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
Benzalkonium Chloride 0.13%
Purppose
Antiseptic
Uses
- Handwash to help reduce bacteria on the skin that potentially can cause disease.
- Recommended for repeated use.
Warings
For external use only.
When Using This Product
Keep out of eyes. In case of eye contact, flush eyes with water.
Stop Use And Ask A Doctor If
irritation and redness develop or if condition persists for more than 72 hours.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
• Wet hands with water and dispense sufficient amount of product into cupped palm of hand. • Wash both hands thoroughly for 15 seconds. • Rinse under running water and dry thoroughly.
Inactive Ingredients
Water, Sodium Lauryl Ether Sulfate, Cocamide MIPA, Sodium Sulfate, Fragrance, Magnesium Nitrate, Magnesium Chloride, Alcohol Denatured, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone, FD&C Red#4, FD&C Yellow #5
Package Labeling:
Label0 (Label0)
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