Otc - Active Ingredient
ACTIVE INGREDIENT:
Benzalkonium Chloride, 0.133% w/v
Bzk Towelette
FDA Label NDC 0404-5824
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Henry Schein Inc. for the product Bzk Towelette (NDC 0404-5824). 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 otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, principal display panel - pouch label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
PURPOSE:
First Aid Antiseptic
Otc - Keep Out Of Reach Of Children
Caution Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Indications & Usage
USE: Antiseptic Cleansing of face, hands and body without soap and water. Air dries in seconds.
Warnings
DO NOT USE: In the eyes or apply over large areas of the body.
STOP USE: If irritation, redness or other symptoms develop. Consult a doctor if the condition persists or gets worse.
Dosage & Administration
Contains 1 Pad
DIRECTIONS: Tear open packet, unfold and use as washcloth
Inactive Ingredient
INACTIVE INGREDIENT: Distilled Water
Principal Display Panel - Pouch Label
HENRY SCHEIN®
112-5824
NDC 0404-5824-01
BZK
TOWELETTE
Contains Benzalkonium Chloride
For External Use Only
NON-STERILE
Contains
1 Pad
CE
Distributed by:
HENRY SCHEIN INC.
Melville, NY 11747 USA
EC REP
Henry Schein U.K. Holdings Ltd.
Gillingham ME8 0SB U.K.
Principal Display Panel (Pouch Label)
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