Active Ingredient
Benzalkonium chloride 0.13%
Sanitizing Hand Wipes
FDA Label NDC 77642-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Commonwealth Wholesale Corp for the product Sanitizing Hand Wipes (NDC 77642-001). 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, use, 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
Antiseptic
Use
■ Hand sanitizer to help reduce bacteria on the skin. For use when soap and water not available
Warnings
For external use only
When Using This Product
■ Avoid getting into the eyes.
■ In case of eye contact immediately flush eyes thoroughly with water.
Stop Use And Ask A Doctor If
■ Irritation or redness develops
■ Conditions persist for more than 72 hours
■ Redness is present
Keep Out Of Reach Of Children
In case of accidental ingestion contact a doctor or Poison Control Center immediately.
Directions
■ Thoroughly wipe hands with cloth
■ Rub hands together until dry
■ No rinsing required
Other Information
■ Dispose of properly, do not flush
Inactive Ingredients
water, polysorbate 20, glycerin, potassium sorbate, aloe (aloe barbadensis) leaf extract, dihydroacetic acid, phenoxyethanol, citric acid
Package Label
Package Label (Bzkwpepckt)
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