HAND SANITIZER BY CN PHARMA- alcohol liquid

Hand Sanitizer by CN Pharma by

Drug Labeling and Warnings

Hand Sanitizer by CN Pharma by is a Otc medication manufactured, distributed, or labeled by Canadian National Pharma Group Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethanol 80% v/v. 

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 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 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

• 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)

Report any adverse reaction to the FDA Medwatch Adverse Event Reporting Program or to: info@cnpharmagroup.com

Inactive ingredients

Glycerin, Hydrogen Peroxide, Denatonium Benzoate, Water, Fragrance

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

HAND SANITIZER BY CN PHARMA 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77536-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
WATER (UNII: 059QF0KO0R)
MENTHA SPICATA OIL (UNII: C3M81465G5)
EAST INDIAN LEMONGRASS OIL (UNII: UP0M8M3VZW)
LAVENDER OIL (UNII: ZBP1YXW0H8)
TEA TREE OIL (UNII: VIF565UC2G)
EUCALYPTUS OIL (UNII: 2R04ONI662)
COCONUT OIL (UNII: Q9L0O73W7L)
ORANGE OIL (UNII: AKN3KSD11B)
ALOE (UNII: V5VD430YW9)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77536-002-01	60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2020
2	NDC: 77536-002-02	330 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2020
3	NDC: 77536-002-03	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2020
4	NDC: 77536-002-04	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/01/2020

Labeler - Canadian National Pharma Group Inc (204126080)

Establishment
Name	Address	ID/FEI	Business Operations
Canadian National Pharma Group Inc		204126080	manufacture(77536-002)