Sanitizing Wipes
FDA Label NDC 78562-013

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Halpern Import Company for the product Sanitizing Wipes (NDC 78562-013). 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, using this product, stop use and ask a doctor, 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

Active Ingredient

Benalkonium chloride 0.13%

Purpose

Antimicrobial Agent

Use

Decreases bacteria on skin

Warnings

For external use only

Do Not Use

if you are allegic to any of the ingredients.

Using This Product

do not get into eyes. In contact occurs, rinse thoroughly with water.

Stop Use And Ask A Doctor

if irritation or rash develops and continues for more than 72 hours

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away

Directions

  • Tear open packet, remove wipe.
  • Wet hands or surface thoroughly with product and let air dry.
  • Throw used wipe in trash. Do not flush.

Inactive Ingredients

Phenoxyethanol, Ethylhexylglycerin, DDAC, Propylene Glycol, Glycerin, Citrus extract, Aqua

Principal Display Panel

NDC 78562-013-30

PurgeTM

SANITIZING WIPES

KEEP OUT OF REACH OF CHILDREN

CAUTION: SEE BACK PANEL FOR ADDITIONAL PRECAUTIONARY STATEMENTS

*NOT TO BE USED AS A DIAPER WIPE

30 WET WIPES - 5.75'' X 9 ''

Label (30)

Label (30)

* Please review the disclaimer below.