1.8OZ HAND SANITIZER WITH CLIP -ASSORTED

Manufacturer: Ningbo Liyuan Daily Chemical Products Co., Ltd.
Effective date: 2017-01-01
Label type: HUMAN OTC DRUG LABEL
Version: 12
Source: legacy-cache
Hydrated at: 2026-08-02 01:03:26

Label at a glance#

Product1.8OZ HAND SANITIZER WITH CLIP -ASSORTED

Active ingredientALCOHOL

Label structure10 sections

Indications and uses

Hand Sanitizer to help reduce bacteria on skin.

Dosage and administration

Wet hands thoroughly with product and rub into the skin until dry. Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Ethyl Alcohol 62.0%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

OTC - PURPOSE SECTION

Hand Sanitizer to help reduce bacteria on skin.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from hear or flame.

When using this product

INDICATIONS & USAGE SECTION

avoid contact with face, eyes, and 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

if irritation redness develops.

Keep out of reach of children.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and rub into the skin until dry.

Children under 6 years of age should be supervised when using this product.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

Products#

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

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

1.8OZ HAND SANITIZER WITH CLIP -ASSORTED
ethyl alcohol
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76176-033	76176-033-01

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
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT

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
64fdd4c0-f44d-0df4-e053-2991aa0a4af1			547fa665-32fd-0cc2-e054-00144ff8d46c	2017-01-01	Warnings	Exact identifier spl id: 64fdd4c0-f44d-0df4-e053-2991aa0a4af1 spl set id: 547fa665-32fd-0cc2-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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