Antibacterial Wet Wipes
FDA Label NDC 69394-005

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Aakron Rule Corporation for the product Antibacterial Wet Wipes (NDC 69394-005). 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, otc - keep out of reach of children, directions, inactive ingredients, product label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Benzalkonium Chloride (0.13%)

Purpose

Antiseptic

Use

For hand-washing to decrease bacteria on skin

Warnings

  • Flammable. Keep away from heat and flame.
  • For External use only.
  • Do not usein eyes. In case of contact, rinse thoroughly with water.
  • Stop use & ask doctorif rash/redness or irritation appears/develops and persist for more than 72 hours.

Otc - Keep Out Of Reach Of Children

Keep out of reach of childrenexcept under adult supervision.If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Slowly peel back label and use one wipe. Reseal, keep closed to prevent evaporation.
  • Thoroughly wipe hands, allow to dry out rinsing. 
  • Discard after single use.

Inactive Ingredients

Water, phenoxyethanol, ethylhexyl glycerin, didecyldimonium chloride, propylene glycol, glycerin, fragrance.

Product Label

Image Description (Image 1 Updated)

Image Description (Image 1 Updated)

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