FDA.reportPublic FDA data

MOSAIC 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 21:46:46

Label at a glance#

ProductMOSAIC Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

Wet hands thoroughly with product and rub into skin until dry. Children 6 years and younger need adult supervision when using this product.

Storage and handling

Store at temperatures not exceeding 30°C. Keep tightly closed.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% ± 5% (v/v)

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Reduces bacteria and viruses on the hands that may cause disease.

PRECAUTIONS

WARNINGS SECTION

  • If taken internally, consult a physician. Keep out of reach of children.
  • FLAMMABLE: Keep away from open flame.
  • FOR EXTERNAL USE ONLY.

WHEN USING THIS PRODUCT: Avoid contact with eyes and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.
S top use and ask doctor If, Irritation or redness 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 into skin until dry. Children 6 years and younger need adult supervision when using this product.

STORAGE

STORAGE AND HANDLING SECTION

  • Store at temperatures not exceeding 30°C.
  • Keep tightly closed.

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100 mL

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80204-001-012022-03-07C16284748780-1d6a99b39-45d9-a426-e053-dadaa90af4c261f19d8f-befb-4a55-8795-2fb4db67a9db
80204-001-012022-01-28C16284748780-1d6a99b39-45d9-a426-e053-dadaa90af4c261f19d8f-befb-4a55-8795-2fb4db67a9db

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
80204-00180204-001-01

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
PROPYLENE GLYCOL6DC9Q167V3IACT
TROLAMINE9O3K93S3TKIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
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
7105d4aa-ebc0-4f25-b570-4011bc42e22761f19d8f-befb-4a55-8795-2fb4db67a9db2022-11-18WarningsExact identifier
spl id: 7105d4aa-ebc0-4f25-b570-4011bc42e227
spl set id: 61f19d8f-befb-4a55-8795-2fb4db67a9db

Reported adverse events (FAERS/openFDA)#

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