Drug Facts

Active ingredient

Benzalkonium chloride 0.13%

Purpose

Antiseptic

Use

For hand washing to decrease bacteria on the skin

Warnings

For external use only.

Do not use

in the eyes

Stop use and ask a doctor if

irritation and redness develop
condition persists for more than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Wet hands thoroughly with product and allow to dry without wiping.

Other information

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

Inactive ingredients

Glycerin, hydroxyethyl cellulose, reverse osmosis water.

Questions or Comments?

(866) 322-7326

Package Labeling:59ml

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Package Labeling:237ml

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Package Labeling:500ml

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Package Labeling:1L

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CARE AND CO HAND SANITIZER
benzalkonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:80755-000
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:80755-000-01	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/15/2020
2	NDC:80755-000-02	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/15/2020
3	NDC:80755-000-03	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/15/2020
4	NDC:80755-000-04	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/15/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	10/15/2020

Labeler - CARE AND COMPANY USA. LLC (107409020)

Care & Co Hand Sanitizer Gel