Bzk Sanitizing Hand Wipe
FDA Label NDC 81529-004

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Premium Ppe, Llc for the product Bzk Sanitizing Hand Wipe (NDC 81529-004). 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 directions for use:, active ingredient:, purpose:, uses:, inactive ingredients:, warnings:, do not use, when using this product,, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Directions For Use:

Wipe liberally over the hands, rub into skin until dry. Recommended for single use.

Active Ingredient:

Benzalkonium Chloride 0.13%

Purpose:

Antiseptic/ hand and skin sanitizer

Uses:

Cleans and sanitizes the skin and decreases bacteria. Recommended for single use.

Inactive Ingredients:

Aloe Barbadensis leaf extract, Aqua, Citric Acid, Caprylyl Glucoside, L a u r e t h - 4 , P o l y h e x a n i d e , Phenoxyethanol, Trielhoxysilylpropyl
Steardimonium Chloride.

Warnings:

Do not freeze

+ For external use only 

Do Not Use

+ in ears, eyes or mouth

When Using This Product,

+avoid contact with the eyes

+ In case of contact, flush eyes with water

Stop Use And Ask A Doctor If

+redness or irritation develops and persists for more than 72 hours

Keep Out Of Reach Of Children

+Children should be supervised when using this product.

Questions?

1-800-920-7650 Mon-Fri 10AM-4PM (EST)

Package Labeling:

Bottle5 (Bottle5)

Bottle5 (Bottle5)

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