FOAMING ANTIBACTERIAL HANDSOAP- benzalkonium chloride liquid

Foaming Antibacterial Handsoap by

Drug Labeling and Warnings

Foaming Antibacterial Handsoap by is a Otc medication manufactured, distributed, or labeled by Chemcor Chemical Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Uses

• Antibacterial foaming hand cleaner.
• Use in daycare, hospitals, nursing homes, physician offices, dental offices and clinics.

Warnings

• For external use only.
• Avoid contact with eyes.
• If contact occurs, rinse thoroughly with water.
• Discontinue use if irritation to redness develops.
• If irritation persists for more than 72 hours, consult a physician.

• KEEP OUT OF REACH OF CHILDREN.
• If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Read the entire label before using this product.
• Ready to use without dilution.
• Dispense 2 pumps of product onto palm of hand and scrub thoroughly over all surfaces of both hands.
• Rinse with clean water and dry.

Inactive Ingredients

Water, Cocamidopropyl Betaine, Caprylyl Glucoside, Glycerine, Tetrasodium EDTA, Benzisothiazol, Methylisothiozol, Fragrance, Citric Acid, Aloe Vera, Yellow #5, Red #40

SPL UNCLASSIFIED SECTION

moisturizes
hard on germs
tough on surface bacteria

CHEMCOR

CHEMICAL CORP

CHINO, CA 91710

CHEMCORCHEMICAL.COM

WARNING
Keep out of reach of children.
May be harmful if swallowed.
May cause irritation to eyes.

institutional & commercial antibacterial hand cleanser

DESCRIPTION
An effective antibacterial foaming hand and skin cleanser which contains benzalkonium chloride, an outstanding germ fighter. Formulated to be tough on bacteria and germs. Regular use of this antibacterial handsoap decreases bacteria levels on the skin and helps reduce risk of infection. Produces rich moisturizing lather to promote complete gentle cleansing. Leaves the skin clean, soft and refreshed. May be used in all types of foaming dispensing units.

Before discarding container, rinse with water.
For institutional and commercial use.
Antes de descargar el contenedor, enjuague con agua.
Para uso institucional y comercial.

Antibacterial Foaming Handsoap

INGREDIENTS AND APPEARANCE

FOAMING ANTIBACTERIAL HANDSOAP 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68041-512
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.0013 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCERIN (UNII: PDC6A3C0OX)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
MAGNESIUM NITRATE (UNII: 77CBG3UN78)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C RED NO. 40 (UNII: WZB9127XOA)
EDETATE SODIUM (UNII: MP1J8420LU)
WATER (UNII: 059QF0KO0R)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Product Characteristics
Color	orange	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68041-512-01	3780 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/15/2020
2	NDC: 68041-512-55	207900 mL in 1 DRUM; Type 0: Not a Combination Product	07/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/15/2020

Labeler - Chemcor Chemical Corporation (018129978)

Establishment
Name	Address	ID/FEI	Business Operations
Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.		028311595	manufacture(68041-512) , api manufacture(68041-512) , pack(68041-512)