FDA.reportPublic FDA data

Tazza

Manufacturer
Tazza Brands East Inc.
Effective date
2025-12-23
Label type
HUMAN OTC DRUG LABEL
Version
19
Source
full-release
Hydrated at
2026-06-01 01:28:20

Label at a glance#

ProductTazza
Active ingredientALCOHOL
Label structure15 sections

Storage and handling

Other information • store below 100℉ (38°C) • non-staining; may discolor some fabrics

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Ethyl Alcohol 70%

OTC - PURPOSE SECTION

Purpose

Antiseptic

INDICATIONS & USAGE SECTION

Uses · to decrease bacteria on the skin

· recommended for repeated use

WARNINGS SECTION

​ Warnings

For external use only

Flammable, keep away from fire or flame

OTC - WHEN USING SECTION

When using this product keep away from eyes.

In case of eye contact, rinse eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness

develop or last more than 72 hours

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

· rub wipe thoroughly over all surface of both hands

· allow to dry without wiping

· supervise children under 6 years old

· not recommended for infants

· dispose of wipe in trash; do not flush

STORAGE AND HANDLING SECTION

Other information • store below 100℉ (38°C)

• non-staining; may discolor some fabrics

INACTIVE INGREDIENT SECTION

Inactive ingredientsAloe Barbadensis Leaf Juice, Decyl Glucoside, Glycerin, Propylene Glycol, Purified Water

SPL UNCLASSIFIED SECTION

Manufactured for

Tazza Brands East

4140 Mound Road

Joliet, IL 60436

A Product of Terraboost®

877-837-7210 • www.tazzabrands.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

tazza-X HAND SANITIZING WIPES
70% Alcohol Formula
Kills Germs
1200 Wet Wipes
4.3 in. x 7.7 in. (11 cm x 18 cm)
NDC: 76370-0004-3

1200 Label 21200 Label 2

1200 Label 11200 Label 1

Pouches

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

76370-0004 - CH76370-0004 - CHAlcohol Wipes-PouchAlcohol Wipes-Pouch

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

80 PACK

NDC: 76370-0004-6

80 Label80 Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1489307ethanol 70 % Medicated PadPSN19
1489307ethanol 0.7 ML/ML Medicated PadSCD19
1489307ethanol 70 % Medicated PadSY19
1489307ethanol 70 % Medicated WipesSY19
1489307ethyl alcohol 70 % ClothSY19

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130860003571439GTIN-13: 0860003571439
EAN-13: 0860003571439
GTIN-12: 860003571439
UPC-A: 860003571439
GTIN storage (14 digits): 00860003571439		Alcohol Wipes Label-80 PACK.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76370-0004-0Tazza40 in 1 POUCHCLOTH4019
76370-0004-0Tazza1.3 mL in 1 APPLICATORCLOTH1.319
76370-0004-1Tazza250 in 1 CANISTERCLOTH25019
76370-0004-1Tazza1.3 mL in 1 APPLICATORCLOTH1.319
76370-0004-2Tazza1500 in 1 BAGCLOTH150019
76370-0004-2Tazza1.3 mL in 1 APPLICATORCLOTH1.319
76370-0004-3Tazza1.3 mL in 1 APPLICATORCLOTH1.319
76370-0004-3Tazza1200 in 1 BAGCLOTH120019
76370-0004-4Tazza1.3 mL in 1 APPLICATORCLOTH1.319
76370-0004-4Tazza240 in 1 CANISTERCLOTH24019
76370-0004-5Tazza160 in 1 POUCHCLOTH16019
76370-0004-5Tazza1.3 mL in 1 APPLICATORCLOTH1.319
76370-0004-6Tazza80 in 1 POUCHCLOTH8019
76370-0004-6Tazza1.3 mL in 1 APPLICATORCLOTH1.319
76370-0004-7Tazza20 in 1 POUCHCLOTH2019
76370-0004-7Tazza1.3 mL in 1 APPLICATORCLOTH1.319
76370-0004-8Tazza50 in 1 POUCHCLOTH5019
76370-0004-8Tazza1.3 mL in 1 APPLICATORCLOTH1.319
76370-0004-9Tazza100 in 1 POUCHCLOTH10019
76370-0004-9Tazza1.3 mL in 1 APPLICATORCLOTH1.319

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76370-000476370-0004-1, 76370-0004-2, 76370-0004-3, 76370-0004-4, 76370-0004-5, 76370-0004-6, 76370-0004-7, 76370-0004-8, 76370-0004-9, 76370-0004-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ALCOHOL3K9958V90MACTIB

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
TazzaETHANOLTazza Brands East Inc.391cc18f-ce63-5d88-e054-00144ff88e882025-12-23WarningsExact identifier
ndc (package): 76370-0004-5
ndc (package): 76370-0004-3
ndc (package): 76370-0004-1
ndc (package): 76370-0004-0
ndc (package): 76370-0004-9
ndc (package): 76370-0004-7
ndc (package): 76370-0004-4
ndc (package): 76370-0004-6
ndc (package): 76370-0004-2
ndc (package): 76370-0004-8
ndc (product): 76370-0004
ndc11 (package): 76370000402
ndc11 (package): 76370000409
ndc11 (package): 76370000400
ndc11 (package): 76370000404
ndc11 (package): 76370000406
ndc11 (package): 76370000405
ndc11 (package): 76370000407
ndc11 (package): 76370000401
ndc11 (package): 76370000403
ndc11 (package): 76370000408
spl id: 46959fc5-3f2c-b47b-e063-6294a90aab13
spl set id: 391cc18f-ce63-5d88-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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