Active ingredient

Benzalkonium chloride 0.11%

Purpose

Antibacterial

Uses

to decrease bacteria on the skin and clean hands
recommended for repeated use

Warnings

For external use only. Flammable, keep away from fire or flame.

Keep out of reach of children.

If accidentally swallowed, get medical help or contact a Poison Control Center right away.

Do not get into eyes. If contact occurs, rinse thoroughly with water.

Discontinue use if irritation or redness develop. If irritation persists for more than 72 hours, consult a doctor.

Directions

apply to hands until thoroughly wet
rub vigorously until dry
supervise children in the use of this product

Inactive Ingredients

Warm Vanilla Sugar

Aqua, Alcohol, Decyl Glucoside, Parfum, Aloe Barbadensis, Methylisothiazolinone, Methylchloroisothiazolinone, Disodium EDTA, Benzophenone-4, Citric Acid, Tocopheryl Acetate, Retinyl Palmitate, Red 33, Blue 1, Yellow 5

Sweet Cherry Blossom

Fresh Ocean Breeze

Cool Cucumber Melon

Irresistible Green Apple

Alluring Red Pomegranate

Sparkling White Cranberry

Crisp White Citrus

Sheer Cotton Whisper

Questions?

1-800-FDA-1088

SATISFACTION GUARANTEED BY REFUND OR EXCHANGE

Made in China

Distributed by Jets, Sets & Elephants Beauty Corp.

For Shopko Stores Operating Co., LLC

Green Bay, WI 54307, U.S.A.

Package/Label Principal Display Panel - Bottle Label

bath+body+etc®

Warm

VANILLA SUGAR

antibacterial

foaming

hand sanitizer

PARABEN FREE

contains aloe vera and

vitamins A & E

1.7 fl oz

Warm Vanilla Sugar Bottle Label

Package/Label Principal Display Panel - Bottle Label

bath+body+etc®

Sweet

CHERRY BLOSSOM

antibacterial

foaming

hand sanitizer

PARABEN FREE

contains aloe vera and

vitamins A & E

1.7 fl oz

Sweet Cherry Blossom Bottle Label

Package/Label Principal Display Panel - Bottle Label

bath+body+etc®

Fresh

OCEAN BREEZE

antibacterial

foaming

hand sanitizer

PARABEN FREE

contains aloe vera and

vitamins A & E

1.7 fl oz

Fresh Ocean Breeze Bottle Label

Package/Label Principal Display Panel - Bottle Label

bath+body+etc®

Cool

CUCUMBER MELON

antibacterial

foaming

hand sanitizer

PARABEN FREE

contains aloe vera and

vitamins A & E

1.7 fl oz

Cool Cucumber Melon Bottle Label

Package/Label Principal Display Panel - Bottle Label

bath+body+etc®

Irresistible

GREEN APPLE

antibacterial

foaming

hand sanitizer

PARABEN FREE

contains aloe vera and

vitamins A & E

1.7 fl oz

Irresistible Green Apple Bottle Label

Package/Label Principal Display Panel - Bottle Label

bath+body+etc®

Alluring

RED POMEGRANATE

antibacterial

foaming

hand sanitizer

PARABEN FREE

contains aloe vera and

vitamins A & E

1.7 fl oz

Alluring Red Pomegranate Bottle Label

Package/Label Principal Display Panel - Bottle Label

bath+body+etc®

Sparkling

WHITE CRANBERRY

antibacterial

foaming

hand sanitizer

PARABEN FREE

contains aloe vera and

vitamins A & E

1.7 fl oz

Sparkling White Cranberry Bottle Label

Package/Label Principal Display Panel - Bottle Label

bath+body+etc®

Crisp

WHITE CITRUS

antibacterial

foaming

hand sanitizer

PARABEN FREE

contains aloe vera and

vitamins A & E

1.7 fl oz

Crisp White Citrus Bottle Label

Package/Label Principal Display Panel - Bottle Label

bath+body+etc®

Sheer

COTTON WHISPER

antibacterial

foaming

hand sanitizer

PARABEN FREE

contains aloe vera and

vitamins A & E

1.7 fl oz

Sheer Cotton Whisper Bottle Label

ANTIBACTERIAL FOAMING HAND SANITIZER
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:50988-190
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.055 mL in 50.275 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955)
SULISOBENZONE (UNII: 1W6L629B4K)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:50988-190-00	50.275 mL in 1 BOTTLE, PUMP

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333E	08/03/2010

ANTIBACTERIAL FOAMING HAND SANITIZER
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:50988-191
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.055 mL in 50.275 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955)
SULISOBENZONE (UNII: 1W6L629B4K)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:50988-191-00	50.275 mL in 1 BOTTLE, PUMP

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333E	08/03/2010

ANTIBACTERIAL FOAMING HAND SANITIZER
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:50988-192
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.055 mL in 50.275 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955)
SULISOBENZONE (UNII: 1W6L629B4K)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:50988-192-00	50.275 mL in 1 BOTTLE, PUMP

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333E	08/03/2010

ANTIBACTERIAL FOAMING HAND SANITIZER
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:50988-193
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.055 mL in 50.275 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955)
SULISOBENZONE (UNII: 1W6L629B4K)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:50988-193-00	50.275 mL in 1 BOTTLE, PUMP

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333E	08/03/2010

ANTIBACTERIAL FOAMING HAND SANITIZER
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:50988-194
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.055 mL in 50.275 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955)
SULISOBENZONE (UNII: 1W6L629B4K)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:50988-194-00	50.275 mL in 1 BOTTLE, PUMP

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333E	08/03/2010

ANTIBACTERIAL FOAMING HAND SANITIZER
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:50988-195
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.055 mL in 50.275 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955)
SULISOBENZONE (UNII: 1W6L629B4K)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
FD&C RED NO. 40 (UNII: WZB9127XOA)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:50988-195-00	50.275 mL in 1 BOTTLE, PUMP

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333E	08/03/2010

ANTIBACTERIAL FOAMING HAND SANITIZER
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:50988-196
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.055 mL in 50.275 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955)
SULISOBENZONE (UNII: 1W6L629B4K)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:50988-196-00	50.275 mL in 1 BOTTLE, PUMP

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333E	08/03/2010

ANTIBACTERIAL FOAMING HAND SANITIZER
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:50988-197
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.055 mL in 50.275 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955)
SULISOBENZONE (UNII: 1W6L629B4K)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:50988-197-00	50.275 mL in 1 BOTTLE, PUMP

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333E	12/01/2010

ANTIBACTERIAL FOAMING HAND SANITIZER
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:50988-198
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.055 mL in 50.275 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955)
SULISOBENZONE (UNII: 1W6L629B4K)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:50988-198-00	50.275 mL in 1 BOTTLE, PUMP

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333E	12/01/2010

Labeler - Jets, Sets, & Elephants Beauty Corp. (243254039)

Name	Address	ID/FEI	Business Operations
Establishment
Gold Orient International Limited		679905914	MANUFACTURE

bath+body+etc® antibacterial foaming hand sanitizer - Warm Vanilla Sugar, Sweet Cherry Blossom, Fresh Ocean Breeze, Cool Cucumber Melon, Irresistible Green Apple, Alluring Red Pomegranate, Sparkling White Cranberry, Crisp White Citrus, Sheer Cotton Whisper

Active ingredient

Purpose

Uses

Warnings

Keep out of reach of children.

Directions

Inactive Ingredients

Warm Vanilla Sugar

Sweet Cherry Blossom

Fresh Ocean Breeze

Cool Cucumber Melon

Irresistible Green Apple

Alluring Red Pomegranate

Sparkling White Cranberry

Crisp White Citrus

Sheer Cotton Whisper

Questions?

SATISFACTION GUARANTEED BY REFUND OR EXCHANGE

Package/Label Principal Display Panel - Bottle Label

Package/Label Principal Display Panel - Bottle Label

Package/Label Principal Display Panel - Bottle Label

Package/Label Principal Display Panel - Bottle Label

Package/Label Principal Display Panel - Bottle Label

Package/Label Principal Display Panel - Bottle Label

Package/Label Principal Display Panel - Bottle Label

Package/Label Principal Display Panel - Bottle Label

Package/Label Principal Display Panel - Bottle Label