ANTIBACTERIAL HANDWASH- benzalkonium chloride liquid

ANTIBACTERIAL HANDWASH by

Drug Labeling and Warnings

ANTIBACTERIAL HANDWASH by is a Otc medication manufactured, distributed, or labeled by Click Products LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

USES

• For Handwashing to decrease bacteria on the skin

WARNING

For external use only.

WHEN USING

• avoid contact with eyes.
• In case of eye contact, flush with water

Stop use and ask a doctor if

• If irritation and redness develops.

KEEP OUT OF REACH OF CHILDREN.

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

DIRECTIONS

• Pump into hands ,wet as needed
• lather vigorously for at least 15 seconds
• Wash skin, rinse throughly and dry.

Inactive Ingredients:

Water（Aqua),Cocamidopropyl Betaine,Sodium Chloride,Fragrance, Citric Acid,Methylchloroisothiazolinone,Methylisothiazolinone,  Cocamide/DEA,D&C Orange No4 , FD&C Blue No1, Glycerin ,Parfum,Tetrasodium EDTA,Sodium laureth sultate.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL HANDWASH 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71611-069
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
COCO DIETHANOLAMIDE (UNII: 92005F972D)
DMDM HYDANTOIN (UNII: BYR0546TOW)
D&C ORANGE NO. 4 (UNII: Q1LIY3BO0U)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
GLYCERIN (UNII: PDC6A3C0OX)
EDETATE SODIUM (UNII: MP1J8420LU)
SULISOBENZONE (UNII: 1W6L629B4K)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
BENZYL ALCOHOL (UNII: LKG8494WBH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71611-069-50	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/26/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/26/2020

Labeler - Click Products LLC (080766174)

Registrant - Click Products LLC (080766174)