DIVINE TREE HAND CLEAN GEL 500ML- ethyle alcohol liquid

Divine Tree Hand Clean Gel 500ml by

Drug Labeling and Warnings

Divine Tree Hand Clean Gel 500ml by is a Otc medication manufactured, distributed, or labeled by K.BIOCOS. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Active Ingredient-Ethyl Alcohol 70% v/v.

Purpose

Purpose-Antiseptic

Use(s)

Use(s) Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

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

Do Not Use

Do Not Use

▪in children less than 2 months of age
▪on open skin wounds

When Using this product

When Using this product- keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop Use and ask a doctor

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

Keep out of reach of children

Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Directions Place enough product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

​Other Information

▪ Store between 15-30C (59-86F)
▪ Avoid freezing and excessive heat above 40C (104F)

Inactive Ingredients

Inactive Ingredients-Water, Glycerin, Carbomer, Triethanolamine, PEG-60 Hydrogenated Castor Oil, PEG-40 Hydrogenated Castor Oil, Hydroxyethylcellulose, Mentha Arvensis Leaf Oil, Sodium Phytate, Sodium Hyaluronate, Panthenol
Scutellaria Baicalensis Root Extract, Portulaca Oleracea Extract, Aloe Barbadensis Leaf Extract

Questions or Comments

Questions or Comments-1-800-819-4159

Principal Display Panel

Principal Display Panel

INGREDIENTS AND APPEARANCE

DIVINE TREE HAND CLEAN GEL 500ML 
ethyle alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73494-502
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	350 mL  in 500 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	144.38 mL  in 500 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73494-502-03	20 in 1 CASE	04/10/2020
1	NDC: 73494-502-02	24 in 1 CASE
1	NDC: 73494-502-01	500 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/10/2020

Labeler - K.BIOCOS (695640141)