POLAR PURE HAND SANITIZER- alcohol liquid

Polar Pure Hand Sanitizer by

Drug Labeling and Warnings

Polar Pure Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by 11569635 Canada Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

ACTIVE INGREDIENTS:

Ethyl alcohol 70% v/v

PURPOSE:

Antimicrobial

USE:

Hand sanitizer to help reduce bacteria on the skin that could cause disease.Recommended for repeated use.

WARNINGS:

Flammable, keep away from fire or flame. For external use only.

When using this product

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor

if irritation or rash appears and lasts.

Keep out of reach of children, 

if swallowed get medical help or contact a poison control center right away

DIRECTIONS:

Place enough product in your palm to thoroughly cover your hands. Rub hands briskly until dry. Children under 6 years of age should be supervised when using this product.

OTHER INFORMATION:

Store below 43 C (110 F). May discolor certain fabrics or surfaces.

INACTIVE INGREDIENTS:

Water (Aqua), Glycerin, Carbomer, Triethanolamine

QUESTIONS?

1-800-772-5513

Package Labeling:59ml

Package Labeling:236ml

Package Labeling:500ml

Package Labeling:1000ml

Package Labeling:4000ml

INGREDIENTS AND APPEARANCE

POLAR PURE HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80608-000
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
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80608-000-01	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2020
2	NDC: 80608-000-02	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2020
3	NDC: 80608-000-03	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2020
4	NDC: 80608-000-04	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2020
5	NDC: 80608-000-05	4000 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	09/01/2020

Labeler - 11569635 Canada Inc (204190615)