ANTIBACTERIAL HANDWASH BERRY MEDLEY- benzalkonium chloride liquid

ANTIBACTERIAL HANDWASH by

Drug Labeling and Warnings

ANTIBACTERIAL HANDWASH by is a Otc medication manufactured, distributed, or labeled by Ningbo Liyuan Daily Chemical Products Co., Ltd., Ningbo Liyuan Daily Chemical Products Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

USES

for hand washing to decrease bacteria on the skin.

WARNING

For external use only.

WARNINGS

When using this product avoid contact with eyes. In case of eye contact, flush with clean water.

STOP USE

and ask a doctor 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
• lather vigorously for at least 5 seconds
• rinse and dry thoroughly.

Inactive Ingredients:

Water（Aqua),Sodium Laureth Sulfate,Cocamidopropyl Betaine,Coconut Monoethanol Amide,Sodium Chloride,Fragrance,Citric Acid,Methylchloroisothiazolinone,Methylisothiazolinone,D&C Red No.33,FD&C Blue No.1.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL HANDWASH  BERRY MEDLEY
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76176-044
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 SULFATE (UNII: BPV390UAP0)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
COCO DIETHANOLAMIDE (UNII: 92005F972D)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76176-044-01	400 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/01/2018

Labeler - Ningbo Liyuan Daily Chemical Products Co., Ltd. (530766098)

Registrant - Ningbo Liyuan Daily Chemical Products Co., Ltd. (530766098)

Establishment
Name	Address	ID/FEI	Business Operations
Ningbo Liyuan Daily Chemical Products Co.,Ltd.		530766098	manufacture(76176-044)