FDA.reportPublic FDA data

GRANDWAY HAND SANITIZER 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 23:38:56

Label at a glance#

ProductGRANDWAY HAND SANITIZER 8OZ
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

Helps reduce bacteria on the skin.

Dosage and administration

Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry. Children under 6 years of age should be supervised when using this product.

Storage and handling

Store below 106 Fahrenheit (41 Degree Celsius) May discolor certain fabrics or surfaces.

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

Helps reduce bacteria on the skin.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only.

When using this product,

OTC - WHEN USING SECTION

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask doctor if irritation or rash appears and lasts.

Keep out of reach for children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry.
  • Children under 6 years of age should be supervised when using this product.

Other Information

STORAGE AND HANDLING SECTION

Store below 106 Fahrenheit (41 Degree Celsius)

May discolor certain fabrics or surfaces.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

water (aqua), carbomer, fragrance, glycerin, propylene glycol, triethanolamine, tocophereyl acetate (vitamin E), aloe barbadensis leaf juice

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

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
76176-19576176-195-01

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
NameUNIIKind
PROPYLENE GLYCOL6DC9Q167V3IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALOE VERA LEAFZY81Z83H0XIACT
CARBOMER 934Z135WT9208IACT
TRIETHANOLAMINE BENZOATEM3EN4GC19WIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
a1bce9c4-df1c-4d08-e053-2a95a90a76f8a1bce9b2-d48c-0a5e-e053-2995a90a7ab02020-03-01WarningsExact identifier
spl id: a1bce9c4-df1c-4d08-e053-2a95a90a76f8
spl set id: a1bce9b2-d48c-0a5e-e053-2995a90a7ab0

Reported adverse events (FAERS/openFDA)#

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