Antibacterial Wet Wipes
FDA Label NDC 73796-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Prostock Llc for the product Antibacterial Wet Wipes (NDC 73796-001). 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, uses, warnings, do not use, stop use & ask doctor, keep out of reach from children, directions, 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

Uses

For hand-washing to decrease bacteria on skin

Warnings

Flammable. Keep away from heat and flame.

For External use only.

Do Not Use

in eyes. In case of contact, rinse thoroughly with water.

Stop Use & Ask Doctor

if rash/redness or irritation appears/develops and persist for more than 72 hours.

Keep Out Of Reach From Children

except under adult supervision. If swallowed, get medical help or contact a Poison Control Center

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

  • Do not flush down toilet.
  • Keep away from sunlight. Store at room temperature 20°-25°Celsius (68°-77° Fahrenheit)
  • May discolor certain fabrics

    • Aqua, Glycerin, Phenoxyethanol, Benzoic Acid, Polysorbate 20, Aloe Barbadensis Leaf Juice, Sodium Citrate

Package Labeling:73796-001-02

Label (Label)

Label (Label)

Package Labeling:73796-001-04

Label2 (Label2)

Label2 (Label2)

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