Active Ingredient
Benzalkonium Chloride 0.13% w/w
Antibacterial Foamsoap
FDA Label NDC 84194-751
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ferguson Enterprises for the product Antibacterial Foamsoap (NDC 84194-751). 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 active ingredient, uses, warnings, directions, inactive ingredients, purpose, keep out of reach of children, label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses
Antibacterial skin cleanser
Effective in destroying harful bacteria to prevent antibacterial cleansing
Warnings
For external use only.
When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs.
Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Read entire label before using this product.
Apply 5 milliliters (teaspoonful) or palmful to hands and forearms.
Scrub thoroughly for 20 seconds and rinse with clean water.
Inactive Ingredients
Aloe Barbadensis Leaf Juice, Citric Acid, FD&C Red 40, FD&C Yellow 5, Fragrance, Glycerin, Laurmine Oxide, Methylchloroisothiazolinone, Methylisothiazolinone, Tetrasodium Glutamate Diacetate, Water
Purpose
Antibacterial
Keep Out Of Reach Of Children
Keep out of the reach of children
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