FDA.reportPublic FDA data

Green supply Hand Sanitizer

Manufacturer
Zhejiang Meizhiyuan Cosmetics Co., Ltd | Townley Inc.
Effective date
2020-04-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:36:44

Label at a glance#

ProductGreen supply Hand Sanitizer 01
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

Apply onto hands/skin, rub until dry.

Label contents#

Full prescribing information#

Drug facts

DESCRIPTION SECTION

Kills 99.9% of germs

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Medicical Ingredient Purpose

Ethyl Alcohol 70-75% Antimicrobial

use

OTC - PURPOSE SECTION

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

DOSAGE & ADMINISTRATION SECTION

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

warnings

WARNINGS SECTION

For External Use Only.

Flammable: Keep away from heat or flame.

OTC - DO NOT USE SECTION

Do not use in Children less tan 2 months of age or on open skin wounds.

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop and ask a doctor if irritation occurs. These may be signs of a serious condition.

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.

Directions

INDICATIONS & USAGE SECTION

Apply onto hands/skin, rub until dry.

Other information

OTHER SAFETY INFORMATION

Store between 15~30 oC (58~86 o F)

Avoid freezing and excessive heat above 40 oC (104 oF)

Non-Medicinal

INACTIVE INGREDIENT SECTION

Water( aqua), Glycerin, propylene glycol, triethanolamine, carbomer, Aloe Barbadensis( Aloe Vera) gel, tocopheryl acetate( vitamin E)

OTC - QUESTIONS SECTION

Questions? 1-888-373-0001

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

54304-021-0154304-021-01

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
54304-02154304-021-01

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

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
aa734723-4bd3-a016-e053-2995a90aab50a2e7e2ba-e8de-d2cc-e053-2995a90a4f972020-07-14WarningsExact identifier
spl set id: a2e7e2ba-e8de-d2cc-e053-2995a90a4f97

Reported adverse events (FAERS/openFDA)#

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