FDA.reportPublic FDA data

76370-0042 tazza 63% alcohol foam sanitizer

Manufacturer
Tazza Brands East, Inc.
Effective date
2026-06-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-06-16 05:10:12

Label at a glance#

Producttazza 63% alcohol foam sanitizer
Active ingredientALCOHOL
Label structure11 sections

Storage and handling

Other information · Store at room temperature. · Avoid excessive heat.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Ethanol 63% V/V

OTC - PURPOSE SECTION

Purpose

Antimicrobial

INDICATIONS & USAGE SECTION

Uses · Decreases bacteria on hands

WARNINGS SECTION

Warnings Flammable: Keep away from flame or high heat.

For external use only

OTC - WHEN USING SECTION

· When using this product keep out of eyes. Stop use and ask a doctor if redness or irritation develops.

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.

OTC - DO NOT USE SECTION

Do not use: on children under 2 years of age unless directed by a doctor.

DOSAGE & ADMINISTRATION SECTION

Directions

· Dispense an adequate amount in your palm to cover all surfaces of both hands completely · Rub hands together until dry.

STORAGE AND HANDLING SECTION

Other information · Store at room temperature.

· Avoid excessive heat.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Water, Cocamidopropylamine Oxide, Dimethicone, Propylene Glycol, Glycerine,Vitamin E

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

tazza 63% alcohol foam sanitizer 1L (33.8 FL OZ)

NDC: 76370-0042-0

1L Label1L Label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeCode 128850029021520tazza 63 alcohol foam sanitizer Label.jpg

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76370-004276370-0042-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
DIMETHICONE92RU3N3Y1OIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
COCAMIDOPROPYLAMINE OXIDEM4SL82J7HKIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
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 63% alcohol foam sanitizerETHANOLTazza Brands East, Inc.53f19eae-7e6f-bdee-e063-6294a90a82c72026-06-11WarningsExact identifier
ndc (package): 76370-0042-0
ndc (product): 76370-0042
ndc11 (package): 76370004200
spl id: 53f19eae-7e70-bdee-e063-6294a90a82c7
spl set id: 53f19eae-7e6f-bdee-e063-6294a90a82c7

Reported adverse events (FAERS/openFDA)#

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