ECOLOGICAL ALCOHOL FREE HAND SANITIZER- benzalkonium chloride gel

Ecological Alcohol Free Hand Sanitizer by

Drug Labeling and Warnings

Ecological Alcohol Free Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by HUNTER AMENITIES INTL. LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient (v/v)

Benzalkonium Chloride 0.13 %

Purpose

Antiseptic skin cleanser

Uses

Antiseptic (skin) cleanser Medicated (skin) cleanser Antibacterial (skin) cleanser
Kills harmful bacteria/germs Effective in destroying (harmful) bacteria to provide antiseptic cleansing For personal hand hygiene to help prevent the spread of bacteria

Warnings

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 swallowed, call a poison control centre or get medical help right away.

Directions

Adults and children over 2 years: For occasional and personal domestic use.  Supervise children when they use this product. Rub thoroughly into hands for at least 30 seconds. Allow to dry.

Inactive ingredients

Aqua/Water/Eau, Propylene Glycol, Glycerin, Hydroxyethylcellulose, Phenoxyethanol, Ethylhexylglycerin, Aloe Barbadensis Leaf Juice

Questions?

1-800-668-1483

Package Labeling:

INGREDIENTS AND APPEARANCE

ECOLOGICAL ALCOHOL FREE HAND SANITIZER 
benzalkonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65910-005
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65910-005-01	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/01/2020

Labeler - HUNTER AMENITIES INTL. LTD (244071015)