2PACK 2OZ HAND SANITIZER- CLASSIC

Manufacturer
Ningbo Liyuan Daily Chemical Products Co.,Ltd.
Effective date
2017-02-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 01:03:24

Label at a glance#

Product2PACK 2OZ HAND SANITIZER- CLASSIC
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand Santizer to help reduce bacteria on skin.

Dosage and administration

. Place enough Product in your palm to thoroughtly 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℉. (41℃) . May discolor certail fabrics or surfaces

Label contents#

Full prescribing information#

Drug Facts Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62.0%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INSTRUCTIONS FOR USE SECTION

Hand Santizer to help reduce bacteria on skin.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only.

When using this product,

DOSAGE & ADMINISTRATION SECTION

do not use in or near the eyes. In case of contact, rinse eyes thoroughtly with water. Stop use and ask doctor if irritation or rash appears and lasts. Keep out of reach for children.

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

Directions:

INDICATIONS & USAGE SECTION

. Place enough Product in your palm to thoroughtly 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℉. (41℃)

. May discolor certail fabrics or surfaces

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water (Aqua), Aloe Barbadensis Leaf Juice, Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate (Vitamin E), Triethanolamine, FD&C Blue No.1, FD&C Yellow No 5.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76176-56276176-562-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
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
64ff385b-4472-88b3-e053-2991aa0a46e5526f94f8-3648-02e0-e054-00144ff88e882017-02-08WarningsExact identifier
spl id: 64ff385b-4472-88b3-e053-2991aa0a46e5
spl set id: 526f94f8-3648-02e0-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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