FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Tazza Brands East Inc.
Effective date
2024-01-24
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 00:07:49

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure13 sections

Storage and handling

Other information do not store above 100°F (38°C) non-staining may discolor some fabrics

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Ethanol 70%

OTC - PURPOSE SECTION

Purpose

Antiseptic

INDICATIONS & USAGE SECTION

Uses

  • for hand sanitizing 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 avoid contact with eyes. In case of eye contact, flush eyes with water and seek medical help.

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

STORAGE AND HANDLING SECTION

Other information

  • do not store above 100°F (38°C)
  • non-staining
  • may discolor some fabrics

INACTIVE INGREDIENT SECTION

Inactive ingredients

Purified Water, Diethanolamine, Propylene Glycol, Glycerin, Aloe Barbadensis Leaf Juice.

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 formula

Kills 99.99% of Germs

fragrance free

6,000 PUMPS

81.15 Fl.OZ. (2,400mL)

Tazza ALC TW 112017Tazza ALC TW 112017

Tazza ALC 112017USTazza ALC 112017US

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
616805ethanol 70 % Topical FoamPSN8
616805ethanol 0.7 ML/ML Topical FoamSCD8
616805ethanol 70 % Topical FoamSY8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76370-0005-2Hand Sanitizer3785 mL in 1 BOTTLE, SPRAYLIQUID37858
76370-0005-4Hand Sanitizer946 mL in 1 BOTTLE, SPRAYLIQUID9468
76370-0005-5Hand Sanitizer1000 mL in 1 BOTTLE, PLASTICLIQUID10008
76370-0005-6Hand Sanitizer2400 mL in 1 BOTTLE, PLASTICLIQUID24008

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76370-0005HAND SANITIZER (ETHANOL) LIQUID [TAZZA BRANDS EAST INC.]8Legacy NDC, 4 package rows20240125_464f97a0-6263-224f-e054-00144ff8d46c.zip

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
76370-000576370-0005-5, 76370-0005-6, 76370-0005-4, 76370-0005-2

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
DIETHANOLAMINEAZE05TDV2VIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT

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
0fb4403b-2e95-4ca0-e063-6294a90a05ac464f97a0-6263-224f-e054-00144ff8d46c2024-01-24WarningsExact identifier
spl id: 0fb4403b-2e95-4ca0-e063-6294a90a05ac
spl set id: 464f97a0-6263-224f-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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