FDA.reportPublic FDA data

1.8OZ HAND SANITIZER

Manufacturer
Ningbo Liyuan Daily Chemical Products Co., Ltd. | Ningbo Liyuan Daily Chemical Products Co.,Ltd.
Effective date
2023-04-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:48:36

Label at a glance#

Product1.8OZ HAND SANITIZER
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

place enough product in your palm rub hands vigorously children under 6 years of age should be supervised when using this product.

Storage and handling

store below 105℉ (40℃) may discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 62% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

hand sanitizer to help reduce bacteria on the skin that could cause disease.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

do not get into eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash appears and lasts.

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 your palm

rub hands vigorously

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

Other information

STORAGE AND HANDLING SECTION

store below 105℉ (40℃)

may discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, propylene glycol, carbomer, aminomethyl propanol, aloe barbadensis leaf juice, fragrance, tocopheryl acetate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76176-02776176-027-01

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
ALCOHOL3K9958V90MACTIB
CARBOMER 934Z135WT9208IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ALOE VERA LEAFZY81Z83H0XIACT
AMINOMETHYL PROPANEDIOLCZ7BU4QZJZIACT

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
2974f439-40ae-9c78-e063-6394a90adafd27ba496a-ceca-8946-e063-6394a90af8b52024-12-15WarningsExact identifier
spl set id: 27ba496a-ceca-8946-e063-6394a90af8b5

Reported adverse events (FAERS/openFDA)#

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