VERTREE CLEAN HAND SANITIZER GEL- alcohol gel

VERTREE Clean Hand Sanitizer Gel by

Drug Labeling and Warnings

VERTREE Clean Hand Sanitizer Gel by is a Otc medication manufactured, distributed, or labeled by MSP CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethanol 70%

Uses

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Purpose

Antibacterial

Warnings

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

Do not use

• if you are allergic to any of the ingredients
• in children less than 2 months of age
• on open skin wounds

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

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

If pregnant or breast-feeding, ask a health professional before use.

Directions

• Take appropriate amount onto your hand and spread it all the way to fingertips. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Inactive ingredients

Keep out of reach of children

Other Information

Store at temperature between 59F ~ 86F (15C ~ 30C)

May discolor certain fabrics or surfaces

Avoid freezing and excessive heat above 104F (40C)

VERTREE Hand Sanitizer Gel

INGREDIENTS AND APPEARANCE

VERTREE CLEAN HAND SANITIZER GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77949-101
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
ALOE (UNII: V5VD430YW9)
CUPRIC BIS(TRIETHANOLAMINE) (UNII: YBM44X0B6H)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77949-101-01	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/21/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/21/2020

Labeler - MSP CO., LTD. (695013758)