PHARMACY PRESCRIPTION 1.8OZ HAND SANITIZER - ORIGINAL SCENT

Manufacturer
Ningbo Liyuan Daily Chemical Products Co.,Ltd.
Effective date
2018-06-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:54:54

Label at a glance#

ProductPHARMACY PRESCRIPTION 1.8OZ HAND SANITIZER - ORIGINAL SCENT
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

- Helps reduce bacteria on the skin that could cause disease. Recommended for repeated use.

Dosage and administration

Place enough product in palm to thoroughly cover your hands. Rub hands together briskly until dry. Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62.0%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

- Helps reduce bacteria on the skin that could cause disease.

Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

do not use in or near the eyes. In case of eye contact, flush eyes thoroughly with water.

Stop use and ask a doctor if:

OTC - STOP USE SECTION

irritation and redness develops and lasts more than 72 hours.

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 right away.

Directions-

DOSAGE & ADMINISTRATION SECTION

Place enough product in palm to thoroughly cover your hands. Rub hands together briskly until dry.

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

OTHER SAFETY INFORMATION

Other information: Store below 110 Fahrenheit degree (43 degrees Celsius)

May discolor certain fabrics or surfaces.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, Aloe Barbadensis Gel, Carbomer, Fragrance, Glycerin, Triethanolamine, Tocopheryl Acetate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76176-07176176-071-01

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
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
6df1ea82-0e07-6d2e-e053-2991aa0aeb2e6df1ea82-0e14-6d2e-e053-2991aa0aeb2e2018-06-05WarningsExact identifier
spl id: 6df1ea82-0e07-6d2e-e053-2991aa0aeb2e
spl set id: 6df1ea82-0e14-6d2e-e053-2991aa0aeb2e

Reported adverse events (FAERS/openFDA)#

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