SCOTT ANTIMICROBIAL FOAM- benzalkonium chloride solution

SCOTT Antimicrobial Foam by

Drug Labeling and Warnings

SCOTT Antimicrobial Foam by is a Otc medication manufactured, distributed, or labeled by Kimberly-Clark. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active Ingredient

Benzalkonium Chloride 0.1% w/w

Purpose

Antiseptic cleanser

Use

For personal hand hygiene to help prevent the spread of certain bacteria.

Warnings

• For External Use Only. Do not ingest. If swallowed, get medical help or contact a Poison Control Center immediately.
• Use with caution in children.
• Avoid contact with eyes. In contact occurs, flush eyes with water.
• Discontinue use & consult a health care practitioner if irritation develops.

• Keep out of reach of children.

• Do not use if you are allergic to any ingredients.

Directions

Apply small amount and lather in hands for at least 30 seconds.

Adults: Supervise children when using this product. Do not dilute product. For occasional use as needed.

Other Information

• Report serious side effects from this product to 1-877-561-6587

Inactive Ingredients

Aloe Barbadensis Leaf Juice Powder, Citric Acid, Coco-Betaine, Glycerin, Panthenol, Sodium Benzoate, Sodium Chloride, Sodium Hydroxide, Tocopheryl Acetate, Water/Eau.

Questions?

1-888-346-4652

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Distributed in the U.S. by Kimberly-Clark Global Sales, LLC,
Roswell, GA 30076-2199

PRINCIPAL DISPLAY PANEL - 33.8 fl oz Bottle Label

Scott®
Brand

Antimicrobial Foam Soap

Benzalkonium
Chloride Solution, NF

For Domestic / Personal Care Use

Kills 99.9% of most common germs†

1 Liter
(33.8 fl oz)

DIN: 02458675

†Enterococcus faecalis VRE; MDR,
Enterococcus faecium, Pseudomonas aeruginosa,
Escherichia coli, Staphylococcus epidermidis,
Salmonella typhi, Streptococcus pyogenus,
Listeria monocytogenes, Proteus vulgaris,
Salmonella enterica

20-29-382-0-01

INGREDIENTS AND APPEARANCE

SCOTT ANTIMICROBIAL FOAM 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55118-235
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y)	Benzalkonium Chloride	1 mg  in 1000 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Coco-Betaine (UNII: 03DH2IZ3FY)
Glycerin (UNII: PDC6A3C0OX)
Sodium Chloride (UNII: 451W47IQ8X)
Sodium Benzoate (UNII: OJ245FE5EU)
Citric Acid Monohydrate (UNII: 2968PHW8QP)
Aloe (UNII: V5VD430YW9)
Panthenol (UNII: WV9CM0O67Z)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Sodium Hydroxide (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55118-235-63	3 in 1 CARTON	12/01/2016
1	NDC: 55118-235-10	1000 mL in 1 CARTRIDGE; 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	12/01/2016

Labeler - Kimberly-Clark (830997032)