FDA.reportPublic FDA data

Premium Nature Hand Sanitizer

Manufacturer
Zhejiang Meizhiyuan Cosmetics Co., Ltd | Townley Inc.
Effective date
2020-04-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:34:20

Label at a glance#

ProductPremium Nature Hand Sanitizer 01
Active ingredientALCOHOL
Label structure9 sections

Label contents#

Full prescribing information#

Instand Hand Sanitizer

DESCRIPTION SECTION

Helps to reduce germs and bacteria on the skin

Use anytime and place without water or towels

Leaves no stickiness or noticeable residue

Ideal for facilities where hand hygiene is critical

Drug facts

DESCRIPTION SECTION

Kills 99.9% of germs

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Purpose

Ethyl Alcohol 75% Antimicrobial

use

OTC - PURPOSE SECTION

Hand sanitizer to help reduce bacterial on skin that potentially can cause disease.

warnings

WARNINGS SECTION

For External Use Only.

Flammable: Keep away from heat or 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.

Stop and ask a doctor if

OTC - STOP USE SECTION

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 contaol center right away.

INDICATIONS & USAGE SECTION

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping.

USER SAFETY WARNINGS SECTION

Supervise children under 6 years of age when using product to avoid swallowing.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

54304-024-0154304-024-01

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
54304-02454304-024-01

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
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
TROLAMINE9O3K93S3TKIACT
CARBOMER 9404Q93RCW27EIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALCOHOL3K9958V90MACTIB
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
ALOEV5VD430YW9IACT

Source Document#

Source XML · Source PDF

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
aa734723-4bcd-a016-e053-2995a90aab50a414b48c-f876-0c5b-e053-2a95a90a27bd2020-07-14WarningsExact identifier
spl set id: a414b48c-f876-0c5b-e053-2a95a90a27bd

Reported adverse events (FAERS/openFDA)#

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