FDA.reportPublic FDA data

Premium Nature hand sanitizer

Manufacturer
Zhejiang Meizhiyuan Cosmetics Co.,Ltd
Effective date
2022-11-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:46:39

Label at a glance#

ProductPremium Nature hand sanitizer
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

Wet hands thoroughly with product and rub the into skin until dry. children under 6 years of age should be supervised by an adult when using. Other information Store below 110 F (43C). May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v.

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

OTC - WHEN USING SECTION

When using this product avoid contact with face, eyes and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.
Stop use and ask a doctor if irritation or redeness develops.

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 .

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and rub the into skin until dry.
  • children under 6 years of age should be supervised by an adult when using.

Other information

  • Store below 110 F (43C).
  • May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Propylene Glycol, Carbomer, Aminomethyl propanol, Fragrance, Aloe Barbadensis (Aloe Vera) Gel, Tocopheryl Acetate (Vitamin E)

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80204-011-012022-03-07C16284748780-1d6a99b39-79e9-a426-e053-dadaa90af4c22ec76cef-9db6-4711-a6bd-018a830b9cc1
80204-011-012022-01-28C16284748780-1d6a99b39-79e9-a426-e053-dadaa90af4c22ec76cef-9db6-4711-a6bd-018a830b9cc1

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
80204-01180204-011-01

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
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
AMINOMETHYLPROPANOLLU49E6626QIACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
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
945cdcb6-9fb3-436b-bb69-74aee77f0cd42ec76cef-9db6-4711-a6bd-018a830b9cc12022-11-18WarningsExact identifier
spl id: 945cdcb6-9fb3-436b-bb69-74aee77f0cd4
spl set id: 2ec76cef-9db6-4711-a6bd-018a830b9cc1

Reported adverse events (FAERS/openFDA)#

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