FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Meixin Beauty & Health Care Products Co., Ltd.
Effective date
2020-08-10
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:18:48

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Put enough product in your palm to cover hands and rubands together briskly until dry. Children under 6 years of age should be supervised when using.

Storage and handling

Store below 110°F(43°C)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Do not use

OTC - DO NOT USE SECTION

do not use in or near the eyes.

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes.
In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts.

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Put enough product in your palm to cover hands and rubands together briskly until dry.
Children under 6 years of age should be supervised when using.

Other information

STORAGE AND HANDLING SECTION

Store below 110°F(43°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Aloe Vera, Trithanolamine, Vitamine E

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on skin.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30730730930930530530630630830823623659 159 122722730 130 1302302592592100ML100ML5959100100

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78565-00578565-005-01, 78565-005-02, 78565-005-03, 78565-005-04, 78565-005-05, 78565-005-06, 78565-005-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
TROLAMINE9O3K93S3TKIACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL SUCCINATE, D-LU4B53JYVEIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
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
dba88f63-5ca3-caf8-e053-2995a90a526ea980a5b4-d9c9-6c1c-e053-2995a90ac9592022-04-02WarningsExact identifier
spl set id: a980a5b4-d9c9-6c1c-e053-2995a90ac959

Reported adverse events (FAERS/openFDA)#

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