FDA.reportPublic FDA data

Premium Nature Hand Sanitizer

Manufacturer
Zhejiang Meizhiyuan Cosmetics Co., Ltd | Townley Inc.
Effective date
2020-06-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:27:10

Label at a glance#

ProductPremium Nature Hand Sanitizer 01
Active ingredientALCOHOL
Label structure11 sections

Label contents#

Full prescribing information#

Drug facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Purpose

Ethyl Alcohol 75% v/v ....Antimicrobial

USE

OTC - PURPOSE SECTION

Hand sanitizer to help reduce bacteria on the skin that may cause disease.

Warning

WARNINGS SECTION

For external use only.

Flammable, Keep away from heat and flame.

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

Avoid contact with face, eyes and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed get immediate medical help or contact a poison control center.

Direction:

DOSAGE & ADMINISTRATION SECTION

Wet hands with product and rub into skin until dry.

INDICATIONS & USAGE SECTION

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

Other information

OTHER SAFETY INFORMATION

Store below 105 oF (40 oC). May discolot certain fabrics or surfaces.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water( aqua), Propylene Glycol, Glycerin, Carbomer, Fragrance, Aminomethyl Propanol, Aloe Barbadensis( Aloe Vera) Gel, Tocopheryl acetate( vitamin E).

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

54304-073-0154304-073-01

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54304-07354304-073-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER 9404Q93RCW27EIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
AMINOMETHYLPROPANOLLU49E6626QIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALCOHOL3K9958V90MACTIB
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
CYMBOPOGON CITRATUS LEAF06JMS448M5IACT

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
aa77c5a2-691d-7f6e-e053-2a95a90a83d5a7b70813-e9a3-d46d-e053-2a95a90a379d2020-07-15WarningsExact identifier
spl set id: a7b70813-e9a3-d46d-e053-2a95a90a379d

Reported adverse events (FAERS/openFDA)#

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