FDA.reportPublic FDA data

MONDSUB REFRESHING HAND SANITIZER GEL

Manufacturer
Guangzhou Xujohn Bio-Technique Co., Ltd.
Effective date
2021-10-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:21:40

Label at a glance#

ProductMONDSUB Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

▪ Place proper gel in palm, rub hands together briskly until dry. ▪ Children under 6, use only under adult supervision. ▪ Not recommended for infants.

Storage and handling

▪ Do not store above 100°F (38°C). ▪ Harmful to wood finishes and plastics.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

To help reduce bacteria and germs on skin.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only.

Do not use on open skin wounds.

Avoid contact with eyes, ears and mouth.

Stop use and ask a doctor if irritation or rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

▪ Place proper gel in palm, rub hands together briskly until dry. ▪ Children under 6, use only under adult supervision. ▪ Not recommended for infants.

Other information

STORAGE AND HANDLING SECTION

▪ Do not store above 100°F (38°C). ▪ Harmful to wood finishes and plastics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

AQUA, GLYCERIN, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, TRIETHANOLAMINE, TOCOPHERYL ACETATE, ALOE BARBADENSIS LEAF JUICE, MALTODEXTRIN, SODIUM HYALURONATE, POTASSIUM SORBATE, SODIUM BENZOATE.

SPL UNCLASSIFIED SECTION

With Aloe Vera Extract

Effectively Cleans

Protects Health

MADE IN CHINA

Guangzhou Xujohn Bio-Technique Co., Ltd.

No.1 Building, the 7th Yard, Lianda Road,

Huangpu District, Guangzhou, China

TEL: 718-326-9560

DANGER

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75351-78975351-789-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
TROLAMINE9O3K93S3TKIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALOE VERA LEAFZY81Z83H0XIACT
MALTODEXTRIN7CVR7L4A2DIACT
HYALURONATE SODIUMYSE9PPT4THIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
SODIUM BENZOATEOJ245FE5EUIACT

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
3bf73558-b506-40cd-bf46-29bcdc315a667c2266e8-b060-4c19-a632-ad38f970c8102021-10-22WarningsExact identifier
spl id: 3bf73558-b506-40cd-bf46-29bcdc315a66
spl set id: 7c2266e8-b060-4c19-a632-ad38f970c810

Reported adverse events (FAERS/openFDA)#

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