GRANDWAY HAND SANITIZER 1.8OZ

Manufacturer: NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.
Effective date: 2020-03-01
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 23:36:41

Label at a glance#

ProductGRANDWAY HAND SANITIZER 1.8OZ

Active ingredientALCOHOL

Label structure9 sections

Indications and uses

hand sanitizer to help reduce bacteria on the skin.

Dosage and administration

wet hands thoroughly with product and rub into skin until dry. Children under 6 years of age should be supervised by an adult when using.

Label contents#

Full prescribing information#

Drug Facts Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62 percent

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

hand sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from heat and flame.

When using this product, avoid contact with face, eyes and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

Stop use and ask 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 a Poison Control Center.

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands thoroughly with product and rub into skin until dry. Children under 6 years of age should be supervised by an adult when using.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Propylene Glycol, Carbomber, Triethanolamine, Fragrance, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate (Vitamin E)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

Products#

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

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

GRANDWAY HAND SANITIZER 1.8OZ
Ethyl Alcohol
WATER
PROPYLENE GLYCOL
.ALPHA.-TOCOPHEROL ACETATE
ALOE VERA LEAF
CARBOMER 934
TRIETHANOLAMINE BENZOATE
GLYCERIN
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76176-194	76176-194-01

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
Name	UNII	Kind
WATER	059QF0KO0R	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
CARBOMER 934	Z135WT9208	IACT
TRIETHANOLAMINE BENZOATE	M3EN4GC19W	IACT
GLYCERIN	PDC6A3C0OX	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a25bd0f0-6fb0-45e7-e053-2a95a90a36ca			a25bd0f0-6faf-45e7-e053-2a95a90a36ca	2020-03-01	Warnings	Exact identifier spl id: a25bd0f0-6fb0-45e7-e053-2a95a90a36ca spl set id: a25bd0f0-6faf-45e7-e053-2a95a90a36ca

Reported adverse events (FAERS/openFDA)#

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