Otc - Active Ingredient
Benzalkonium Chloride 0.13% -----Sanitizer
Hand Sanitizer Alcohol Free
FDA Label NDC 50157-050
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Brands International Corp for the product Hand Sanitizer Alcohol Free (NDC 50157-050). 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 otc - active ingredient, use, directions, warnings, general warning, inactive ingredients, purpose, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Use
As a sanitizer to help reduce bacteria on the skin
Directions
Put enough product in the palm to cover hands and rub together briskly until the liquid is dry. Children under 6 should be supervised using sanitizer
Warnings
FOR EXTERNALUSE ONLY. avoid contact with eyes. In case of contact with eyes, flush your eyes thoroughly with water. consult your doctor. Discontinue use if skin irritation or redness develops
General Warning
Keep out of reach of children. if swallowed, get medical help or contact poison control center immidiately
Inactive Ingredients
Water, Lauramine oxide, propylene glycol, glycerin, vitamin e, aloe vera leaf extract
Purpose
Sanitizer
Package Label.Principal Display Panel
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