OTC Medication Information: BZK Alcohol Free Hand Sanitizer

BZK ALCOHOL FREE HAND SANITIZER- benzalkonium chloride liquid
Premium PPE, LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Facts

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

Bottle4
(click image for full-size original)

Package Labeling:50ml

Label
(click image for full-size original)

Package Labeling:500ml

Label2
(click image for full-size original)

BZK ALCOHOL FREE HAND SANITIZER
benzalkonium chloride liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:81529-002
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 1.3 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
ALOE VERA LEAF
WATER
CITRIC ACID MONOHYDRATE
CAPRYLYL GLUCOSIDE
LAURETH-4
POLIHEXANIDE
PHENOXYETHANOL
TRIETHOXYSILYLPROPYL STEARDIMONIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:81529-002-02 150 mL in 1 BOTTLE None
2 NDC:81529-002-01 50 mL in 1 BOTTLE None
3 NDC:81529-002-03 500 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 02/03/2020
Labeler — Premium PPE, LLC (117835683)

Revised: 03/2021 Premium PPE, LLC

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2022. All Rights Reserved.