FDA.reportPublic FDA data

tazza HAND SANITIZER

Manufacturer
Tazza Brands East Inc.
Effective date
2025-12-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:28:18

Label at a glance#

Producttazza HAND SANITIZER
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Benzalkonium Chloride 0.13% w/v

OTC - PURPOSE SECTION

Purpose

Antimicrobial

INDICATIONS & USAGE SECTION

Uses For hand sanitizing to decrease bacteria on the skin.

WARNINGS SECTION

Warnings

· For external use only.

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

· Stop use and ask a doctor if irritation or redness develops.

· Keep out of reach of children.

· If swallowed get medical help or contact Poison Control Center right away.

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

· Stop use and ask a doctor if irritation or redness develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

· Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions

· Apply and rub thoroughly over all surfaces of both hands.

· Allow to dry without wiping.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1.0 Gallon
3.78 Liters
NDC: 76370-0032-0

3.78 Liters Label3.78 Liters Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049254benzalkonium chloride 0.13 % Topical SolutionPSN2
1049254benzalkonium chloride 1.3 MG/ML Topical SolutionSCD2
1049254benzalkonium chloride 0.13 % Topical SolutionSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76370-0032-0tazza HAND SANITIZER3.78 L in 1 BOTTLELIQUID3.782

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
76370-003276370-0032-0

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
GLYCERINPDC6A3C0OXIACT
ALOE BARBADENSIS LEAF JUICERUE8E6T4NBIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

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
tazza HAND SANITIZERBENZALKONIUM CHLORIDETazza Brands East Inc.327b9971-808d-ff93-e063-6394a90adce42025-12-24WarningsExact identifier
ndc (package): 76370-0032-0
ndc (product): 76370-0032
ndc11 (package): 76370003200
spl id: 46ad830d-5397-ccbe-e063-6394a90aa594
spl set id: 327b9971-808d-ff93-e063-6394a90adce4

Reported adverse events (FAERS/openFDA)#

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