Bzk Alcohol Free Hand Sanitizer
FDA Label NDC 81529-002
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Premium Ppe, Llc for the product Bzk Alcohol Free Hand Sanitizer (NDC 81529-002). 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 drug facts, active ingredient:, purpose:, uses:, warnings:, do not use, when using this product,, stop use and ask a doctor if, 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:
Hand & Skin Sanitizer
Uses:
BZK™ Alcohol Free Hand Sanitizer provides revolutionary protection in an alcohol-free formula. The scientifically-proven solution kills harmful germs, bacteria, and microbes, and gently soothes and softens skin with aloe vera. Recommended for repeated use.
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.
Directions:
Apply liberally to the palms of the hands or areas of damaged skin. Rub into skin until dry. Recommended for repeated use.
Other Information:
Store in a cool dry place below 104°F(40°C).
Inactive Ingredients:
Aloe Barbadensis leaf extract, Aqua, Citric Acid, Caprylyl Glucoside, Laureth-4, Polyhexanide, Phenoxyethanol, Triethoxysilylpropyl Steardimonium Chloride.
Questions?
1-800-920-7650 Mon-Fri 10AM-4PM (EST)
Package Labeling:150Ml
Package Labeling:50Ml
Package Labeling:500Ml
* Please review the disclaimer below.