Active Ingredient
Benzalkonium Chloride (0.13%)
Benzalkonium Chloride Liquid
FDA Label NDC 72288-021
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Amazon.com Services Llc for the product Benzalkonium Chloride (NDC 72288-021). 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, purpose, uses, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antibacterial.
Uses
For hand washing to decrease bacteria on the skin.
Warnings
For external use only.
When Using This Product
- Avoid contact with eyes. In case of contact, rinse throughly with water.
Stop Use And Ask A Doctor If
- Irritaion or redness develops and lasts for more than 72 hours.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right awsy.
Directions
- Use to refil a foaming hand soap pump bottle.
- Apply onto dry hands. Lather and rinse thoroghly with water,
Inactive Ingredients.
Water (Aqua), Cocamidopropyl Betaine, Glycerin, Fragrance (Parfum), Polysorbate 20, Tetrasodium EDTA, Hydroxyethylcellulose, Decyl Glucoside, Citric Acid, Benzophenone-4, Methylisothiazolinone, Propylene Glycol, Polyquaternium-7, Sodium Citrate, Methylchloroisothiazolinone, Aloe Barbadensis Leaf Juice, Camellia Sinensia Leaf Extract, Blue 1 (CI 42090), Ext.Violet 2 (CI 60730).
Questions?
1-877-485-0385
Ndc-72288-021-32
Principal Display Panel (72288 021 32)
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