DIVINE TREE HAND SANITIZER GEL- ethyl alcolhol liquid

Divine Tree Hand Sanitizer Gel by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose(s)

Purpose-Antiseptic

Use(s)

Use(s)-Health care personnel hand rub to help reduce bacteria that potentially can cause disease.

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, Aminomethyl Propanol, Mentha Arvensis Leaf Oil, Tocopheryl Acetate, Panthenol, Sodium Hyaluronate, Aloe Barbadensis Leaf Extract

Questions Or Comments

Questions Or Comments-1-800-819-4159

Divine Tree Hand Sanitizer Gel 500ml

Divine Tree
Hand Sanitizer Gel
Non-Sterile Solution
Help Reduce Bacteria on the skin
For All Day Use
No Sticky
Deep Moisturizing
500ml 16.9 fl.oz

INGREDIENTS AND APPEARANCE

DIVINE TREE HAND SANITIZER GEL 
ethyl alcolhol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73494-500
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)	144.45 mL  in 500 mL

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73494-500-02	24 in 1 CASE	04/10/2020
1	NDC: 73494-500-01	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)