Cleansense Hand Sanitizer Gel

Cleansense Hand Sanitizer by

Drug Labeling and Warnings

Cleansense Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by KIMIRICA HUNTER INTERNATIONAL LLP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

CLEANSENSE HAND SANITIZER- alcohol gel 
KIMIRICA HUNTER INTERNATIONAL LLP

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Cleansense Hand Sanitizer Gel

Drugs Fact

Active Ingredients(v/v):

Ethyl Alcohol 70%

Purpose

Antiseptic Skin Cleanser

Uses:

-Kill Germs.
-Antiseptic Skin Cleanser.
-Keep your hands moisturized.
-Everyday personal hygiene product.
-Antibacterial property against germs.
-Refreshes hands with its aroma.

Warning:

For external use only.

When using this product

avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask/ consult a doctor

physician/ health care practitioner/ health care provider/ health care professional if irritation develops.

Keep out of reach of children.

If swollowed, call a Poison Control Center or get medical help right away.

Flammability warning.

Keep away from open flame and sources of heat.

Directions:

Adult and children over 2 years:
Supervise children when they use this product.
Squeeze out optimum of sanitizer and rub until hands are dry.

Inactive Ingredients:

Aloe Barbadensis (Aloe Vera) Leaf Extract, Azadirachta Indica (Neem) Leaf Extract, Glycerin, Carbomer, Triethanolamine, Fragrance Q.S., Water (Aqua) Q.S.

Package Labeling:

CLEANSENSE HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79750-000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AZADIRACHTA INDICA LEAF (UNII: HKY915780T)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79750-000-00	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/16/2020	07/31/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/16/2020	07/31/2022

Labeler - KIMIRICA HUNTER INTERNATIONAL LLP (856827349)

Revised: 9/2022

Document Id: e807f3c2-490c-921b-e053-2a95a90af76a

34390-5

Set id: cf0ecf7c-93d0-46f2-aafb-cc7ebbe0bbf4

Version: 4

Effective Time: 20220906