PERSONAL CARE ANTIBACTERIAL FOAMING HAND WILD FLOWERS- benzalkonium chloride liquid PERSONAL CARE ANTIBACTERIAL FOAMING HAND FRESH PICKED STRAWBERRIES- benzalkonium chloride liquid PERSONAL CARE ANTIBACTERIAL FOAMING HAND BEACH BREEZE- benzalkonium chloride liquid PERSONAL CARE ANTIBACTERIAL FOAMING HAND CITRUS SUNSHINE- benzalkonium chloride liquid

Personal CARE Antibacterial by

Drug Labeling and Warnings

Personal CARE Antibacterial by is a Otc medication manufactured, distributed, or labeled by Personal Care Products, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug FactsActive ingredient

Benzalkonium Chloride 0.1%

Purpose

Antibacterial

Keep out of reach of children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Uses

for hand washing to decrease bacteria on the skin.

Warnings

For external use only.

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.

Directions

• pump into hands
• lather vigorously for at least 15 seconds
• rinse and dry thoroughly.

Inactive ingredients

Water (Aqua), Laureth-9, Disodium, Cocoamphodiacetate, Citric Acid, Fragrance, Glycerin, Methylchloroisothiazolinone, Methylisothiazolinone.

Personal CARE ® ANTIBACTERIAL FOAMING Hand Soap LabelsWild FlowersFresh Picked StrawberriesBreach BreezeCitrus Sunshine

Personal CARE ® ANTIBACTERIAL FOAMING Hand Soap

Wild Flowers
Fresh Picked Strawberries
Breach Breeze
Citrus Sunshine

TRICLOSAN FREE
7.5 FL OZ (221.8 mL)

Distributed by: PERSONAL CARE PRODUCTS, LLC

3001 Big Beaver Rd, Ste 520 Troy, MI 43034

Made in China

INGREDIENTS AND APPEARANCE

PERSONAL CARE ANTIBACTERIAL  FOAMING HAND WILD FLOWERS
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 29500-9881
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.0002218 mg  in 221.8 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
LAURETH-9 (UNII: 0AWH8BFG9A)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 29500-9881-1	221.8 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	12/10/2015

PERSONAL CARE ANTIBACTERIAL  FOAMING HAND FRESH PICKED STRAWBERRIES
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 29500-9018
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.0002218 mg  in 221.8 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
LAURETH-9 (UNII: 0AWH8BFG9A)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 29500-9018-1	221.8 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	12/10/2015

PERSONAL CARE ANTIBACTERIAL  FOAMING HAND BEACH BREEZE
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 29500-9020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.0002218 mg  in 221.8 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
LAURETH-9 (UNII: 0AWH8BFG9A)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 29500-9020-1	221.8 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	12/10/2015

PERSONAL CARE ANTIBACTERIAL  FOAMING HAND CITRUS SUNSHINE
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 29500-9319
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.0002218 mg  in 221.8 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
LAURETH-9 (UNII: 0AWH8BFG9A)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 29500-9319-1	221.8 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	12/10/2015

Labeler - Personal Care Products, LLC (966155082)

Registrant - Personal Care Products, LLC (966155082)