Antibacterial Hand Wipes
FDA Label NDC 78711-002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Lidersan Saglik Ve Gida Urunleri Anonim Sirketi for the product Antibacterial Hand Wipes (NDC 78711-002). 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 ingredients, 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

Active Ingredients

Benalkonium chloride (0.13%)

Purpose

Antibacterial

Use

decrease bacteria on skin

Warnings

For external use only

Do Not Use

if you are allergic to any of the ingredients

When Using This Product

donot get into eyes.

if 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:

*adults and children 2 years and over

  • apply to hands 
  • allow to dry without wiping

    • *children under 2 years

    • ask a doctor before use 

Inactive Ingredients

Water, Phenoxyethanol, Polysorbate 20, Gycerin, PEG-7 Glyceryl Cocoate, Cocamidropropyl Betaine, Fragrance, Aloe barbadensis leaf juice, Tocopheryl Acetate, ,Disodium EDTA , Ethylparaben, Citric Acid, Citronellol,Hexyl Cinnamal,Limonene,Linalool, Ethylhexyglycerin

Adverse Reactions

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