Active Ingredients
Benzalkonium Chloride 0.13%
The following Structured Product Label (SPL) was submitted to the FDA by Alo New York Llc for the product Benzalkonium Chloride (NDC 82355-552). 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 ingredients, purpose, uses, warnings, when using this product, stop use and ask a doctor, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Benzalkonium Chloride 0.13%
Antimicrobial
For external use only.
avoid contact with eyes. In case of contact, flush with water.
If redness or irritation develops and persists for more than 72 hours
Children should be supervised when using this product
Take wipe and rub thoroughly over all surface of both hands. Wet hands thoroughly with wipes. Rub hand together briskly to dry without wiping. Dispose of wipe. Do not flush.
Purified Water, Decyl Glucoside, Aloe Barbadensis (Aloe) Leaf Extract, Phenoxyethanol, Citric Acid, Sodium Benzoate, Potassium Sorbate, Eucalyptus Globulus Oil, Mentha Piperita (Peppermint) Oil.
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