Active Ingredient
Benzalkonium chloride 0.1%
Antiseptic Wipes
FDA Label NDC 79299-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Global Inventory Solutions Corp. for the product Antiseptic Wipes (NDC 79299-002). 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, do not use, when using this product, stop use and ask a doctor if, keep out of reach of children, 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
Do Not Use
■ on infants
■ on open skin wounds
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
Other Information
■ dispose of properly, do not flush
Inactive Ingredients
citric acid,disodium EDTA, glycerin, polysorbate 20, tocopheryl acetate
Package Label
Package Label (Antisptcwpesasepso0.1bkc)
* Please review the disclaimer below.
