MONDSUB HAND SANITIZER- alcohol gel

MONDSUB Hand Sanitizer by

Drug Labeling and Warnings

MONDSUB Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Guangzhou Xujohn Bio-Technique Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Alcohol 70%

Purpose

Antiseptic

Use

To help reduce bacteria and germs on skin.

Warnings

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.

Keep out of reach of children.

Directions

▪ 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

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

Inactive ingredients

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

INGREDIENTS AND APPEARANCE

MONDSUB HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75351-789
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
TROLAMINE (UNII: 9O3K93S3TK)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75351-789-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/21/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/21/2020

Labeler - Guangzhou Xujohn Bio-Technique Co., Ltd. (403308789)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Xujohn Bio-Technique Co., Ltd.		403308789	manufacture(75351-789)