ANTIBACTERIAL LAVENDER SCENT- benzalkonium chloride liquid ANTIBACTERIAL LEMON SCENT- benzalkonium chloride liquid ANTIBACTERIAL WATERMELON SCENT- benzalkonium chloride liquid ANTIBACTERIAL- benzalkonium chloride liquid ANTIBACTERIAL COTTON SCENT- benzalkonium chloride liquid

Antibacterial by

Drug Labeling and Warnings

Antibacterial by is a Otc medication manufactured, distributed, or labeled by Protect U Guard LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

Skin Antimicrobial

Uses

reduces amount of bacteria on hands

Warnings

For external use only: hands.

When using this product

do not use in or near eyes. In case of eye contact, flush thoroughly with water. Do not inhale or ingest.

Stop use and ask doctor if

irritation or redness develops. 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

Dispense an adequate amount in your palm to cover all surfaces of both hands completely. Scrub thoroughly for at least fifteen seconds. Rinse completely and dry

Inactive ingredients

Water, Lauramine Oxide, Glycerin, PEG-120 Methyl Glucose Dioleate, Parfum.

Questions or comments?

813-815-0530 or www.protectuguard.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL LAVENDER SCENT 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71788-019
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
WATER (UNII: 059QF0KO0R)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71788-019-70	24 in 1 CARTON	12/02/2021
1	NDC: 71788-019-80	100 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2	NDC: 71788-019-50	12 in 1 CARTON	12/02/2021
2	NDC: 71788-019-60	530 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
3	NDC: 71788-019-10	4 in 1 CARTON	12/02/2021
3	NDC: 71788-019-20	1000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	12/02/2021

ANTIBACTERIAL LEMON SCENT 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71788-018
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
WATER (UNII: 059QF0KO0R)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71788-018-70	24 in 1 CARTON	12/02/2021
1	NDC: 71788-018-80	100 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2	NDC: 71788-018-50	12 in 1 CARTON	12/02/2021
2	NDC: 71788-018-60	530 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
3	NDC: 71788-018-10	4 in 1 CARTON	12/02/2021
3	NDC: 71788-018-20	1000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	12/02/2021

ANTIBACTERIAL WATERMELON SCENT 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71788-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
WATER (UNII: 059QF0KO0R)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71788-020-70	24 in 1 CARTON	12/02/2021
1	NDC: 71788-020-80	100 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2	NDC: 71788-020-50	12 in 1 CARTON	12/02/2021
2	NDC: 71788-020-60	530 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
3	NDC: 71788-020-10	4 in 1 CARTON	12/02/2021
3	NDC: 71788-020-20	1000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	12/02/2021

ANTIBACTERIAL 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71788-017
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
WATER (UNII: 059QF0KO0R)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71788-017-70	24 in 1 CARTON	12/02/2021
1	NDC: 71788-017-80	100 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2	NDC: 71788-017-50	12 in 1 CARTON	12/02/2021
2	NDC: 71788-017-60	530 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
3	NDC: 71788-017-10	4 in 1 CARTON	12/02/2021
3	NDC: 71788-017-20	1000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	12/02/2021

ANTIBACTERIAL COTTON SCENT 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71788-021
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
WATER (UNII: 059QF0KO0R)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71788-021-70	24 in 1 CARTON	12/02/2021
1	NDC: 71788-021-80	100 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2	NDC: 71788-021-50	12 in 1 CARTON	12/02/2021
2	NDC: 71788-021-60	530 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
3	NDC: 71788-021-10	4 in 1 CARTON	12/02/2021
3	NDC: 71788-021-20	1000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	12/02/2021

Labeler - Protect U Guard LLC (080070945)

Establishment
Name	Address	ID/FEI	Business Operations
Protect U Guard LLC		080070945	manufacture(71788-017, 71788-018, 71788-019, 71788-020, 71788-021)