FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
A2Z Products, LLC
Effective date
2021-10-22
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:29:13

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

Hand sanitizer to decrease bacteria on skin.

Dosage and administration

Rub hands thoroughly with this products until try, children younger than 6 should be supervised by an adult when using.

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol, 75% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses:

DOSAGE & ADMINISTRATION SECTION

Hand sanitizer to decrease bacteria on skin.

Warnings:

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

avoid contacting with face, eyes, and broken skin. In case of eye contacting, flush with plenty of water and seek medical attention.

Stop Use and consult a doctor if

OTC - STOP USE SECTION

irritation or redness develops.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swallowed, get medical help or contact Poison Control Center.

Directions:

INDICATIONS & USAGE SECTION

Rub hands thoroughly with this products until try, children younger than 6 should be supervised by an adult when using.

Other Information:

OTHER SAFETY INFORMATION

Store below 105 ºF. May discolor some fabrics.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water (Aqua), Triethanolamine, Polyacrylic Acid, Aloe Barbadensis (Aloe Vera) Gel, Glycerin, Propylence Glycol, Tocophery Acetate (Vitamin E).

GREIGHT Hand Sanitizer - 1fl oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GR8-HS-1GR8-HS-1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72728-004-812021-11-05C16284748780-1c7ccaba7-2730-fd44-e053-dadaa90aa01bGREIGHT Hand Sanitizer - 1fl oz
72728-004-812021-07-23C16284748780-1c7ccaba7-2730-fd44-e053-dadaa90aa01bGREIGHT Hand Sanitizer - 1fl oz

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72728-00472728-004-81

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
AMINOMETHYLPROPANOLLU49E6626QIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
POLYACRYLIC ACID (250000 MW)9G2MAD7J6WIACT

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
cef7d296-299f-5c20-e053-2a95a90a289ba69e1274-2ff5-958e-e053-2a95a90afe7f2021-10-22WarningsExact identifier
spl id: cef7d296-299f-5c20-e053-2a95a90a289b
spl set id: a69e1274-2ff5-958e-e053-2a95a90afe7f

Reported adverse events (FAERS/openFDA)#

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