THEPURI DEEP PURE HAND SANITIZER- ethyl alcohol gel

THEPURI DEEP PURE HAND SANITIZER by

Drug Labeling and Warnings

THEPURI DEEP PURE HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by E.CIS COSMETIC.Co.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 70% v/v..........................Antiseptic

Purpose

Purpose.Antiseptic

Use

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

Warnings

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

Do not use

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

When using

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

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

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

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

Inactive ingredients

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

Package Label - Principal Display Panel

100 mL (3.38 fl. oz.) NDC: 73862-203-10

DEEP PURE HAND SANITIZER NON-STERILE SOLUTION

Help reduce bacteria on the skin

Instant use without water

Non-Sticky

INGREDIENTS AND APPEARANCE

THEPURI DEEP PURE HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73862-203
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)	28.89 mL  in 100 mL

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73862-203-11	60 in 1 CASE	04/13/2020
1	NDC: 73862-203-10	100 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 73862-203-21	24 in 1 CASE	04/13/2020
2	NDC: 73862-203-20	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	04/13/2020

Labeler - E.CIS COSMETIC.Co.,Ltd (689846270)

Establishment
Name	Address	ID/FEI	Business Operations
E.CIS COSMETIC.Co.,Ltd		689846270	manufacture(73862-203)