Benzalkonium Chloride Swab
FDA Label NDC 64709-100

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Diamond Wipes International for the product Benzalkonium Chloride (NDC 64709-100). 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 purpose, active ingredient, uses, directions, warnings, 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

Antimicrobial

Active Ingredient

Benzalkonium Chloride 0.13%

Uses

  • For hand sanitizing to decrease bacteria on the skin
  • Safe for repeated use

Directions

  • Peel back label
  • remove and unfolod wipe
  • wipe hands thoroughly for approximately 30 seconds
  • dispose of used wipe in trash, do not flush

Warnings

For external use only

When using this product avoid contact with eyes, if in eyes rinse thoroughly with water

Discontinue use and ask a doctor if irritation and redness develops and conditions persist for more than 72 hours.

Keep Out Of Reach Of Children

If swollowed, get medical help or contact the Poison Control Center right away.

* Please review the disclaimer below.