FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Tazza Brands East Inc.
Effective date
2025-01-01
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 00:53:28

Label at a glance#

ProductHand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Benzalkonium chloride 0.13%

OTC - PURPOSE SECTION

Purpose

Antimicrobial

INDICATIONS & USAGE SECTION

Uses

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

WARNINGS SECTION

Warnings

For external use only

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develop

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Directions

  • apply liberally into palm of hand
  • rub hands together until dry
  • no need to rinse

INACTIVE INGREDIENT SECTION

Inactive ingredients

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

SPL UNCLASSIFIED SECTION

Manufactured for Terraboost Media, LLC, 3109 Grand Avenue #300, Miami, FL 33133

A Product of Terraboost®

Made in Taiwan [Made in U.S.A.]

www.tazzabrands.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Tazza Instant Hand Sanitizer Foam

alcohol-free

Kills 99.99% of Germs

fragrance free

2,500 PUMPS

33.81 Fl. OZ. (1,000mL)

Tazza_BZK Foam TW 112017Tazza_BZK Foam TW 112017

Tazza_BZK Foam US 112017Tazza_BZK Foam US 112017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1020365benzalkonium chloride 0.13 % Topical FoamPSN6
1020365benzalkonium chloride 1.3 MG/ML Topical FoamSCD6
1020365benzalkonium chloride 0.13 % Topical FoamSY6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76370-0006-1Hand Sanitizer3785 mL in 1 BOTTLELIQUID37856
76370-0006-5Hand Sanitizer1000 mL in 1 BOTTLE, PLASTICLIQUID10006
76370-0006-6Hand Sanitizer2400 mL in 1 BOTTLE, PLASTICLIQUID24006

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76370-0006HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [TAZZA BRANDS EAST INC.]6Legacy NDC, 3 package rows20250124_464f97a0-623a-224f-e054-00144ff8d46c.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76370-000676370-0006-5, 76370-0006-6, 76370-0006-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
DECYL GLUCOSIDEZ17H97EA6YIACT

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
29176154-1b55-742f-e063-6294a90a29dc464f97a0-623a-224f-e054-00144ff8d46c2025-01-01WarningsExact identifier
spl id: 29176154-1b55-742f-e063-6294a90a29dc
spl set id: 464f97a0-623a-224f-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.