Tazza Cloth
FDA Label NDC 76370-0001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Tazza Brands East Inc. for the product Tazza (NDC 76370-0001). 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 other, otc - active ingredient, otc - purpose, indications & usage, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Active ingredient

Benzalkonium Chloride 0.13%

Otc - Purpose

Purpose

Antimicrobial

Indications & Usage

Uses

  • for hand sanitizing to decrease bacteria on the skin
  • recommended for repeated use

Warnings

Warnings

For external use only

Otc - When Using

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

Otc - Stop Use

Stop use and ask a doctor if irritation or redness develop

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Dosage & Administration

Directions

  • take wipe and rub thoroughly over all surfaces of both hands
  • rub hands together briskly to dry
  • dispose of wipe

Inactive Ingredient

Inactive ingredients Purified Water, Glycerin, Aloe Barbadensis Leaf Juice, Decyl Glucoside

Package Label.Principal Display Panel

NDC 76370-0001-3

tazza®

HAND SANITIZING WIPES

Alcohol-Free Formula

Contains Benzalkonium Chloride

Kills 99.99% of most common germs

1200 Wet Wipes

4.3" x 7.1" ((11cm x 18cm)

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