SCOTT ANTIMICROBIAL FOAM SKIN CLEANSER- benzalkonium chloride solution

SCOTT Antimicrobial Foam Skin Cleanser by

Drug Labeling and Warnings

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

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Benzalkonium chloride 0.1 %

Purpose

Antiseptic skin cleanser

Uses

For personal hand hygiene to help prevent the spread of bacteria

Warnings

For external use only

When using this product avoid contact with eyes. If contact occurs, rinse with water.

Stop use and ask a doctor if irritation develops.

Keep out of reach of children.

If swallowed, call a poison control centre or get medical help right away.

Directions

For occasional personal domestic use as needed. Supervise children when they use this product. Lather in hands with water for at least 30 seconds. Rinse well.

Inactive ingredients

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

Questions?

Call 1-888-346-4652

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 1.2 L Bottle Label

91594

Empty &
Discard Pump

PLASTIC
BOTTLE

how2recycle.info

DIN # 02480816

For Personal / Domestic Use Only

Scott®
Brand

Antimicrobial
Foam Skin Cleanser

Benzalkonium Chloride
Solution, USP

SAME GREAT
FORMULATION.
Now Scott®
branded!

RINSE OFF

20-14-700-0-02

1.2 L (40.5 fl oz)

INGREDIENTS AND APPEARANCE

SCOTT ANTIMICROBIAL FOAM SKIN CLEANSER 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55118-800
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
Aloe (UNII: V5VD430YW9)
Citric Acid Monohydrate (UNII: 2968PHW8QP)
Coco-Betaine (UNII: 03DH2IZ3FY)
Glycerin (UNII: PDC6A3C0OX)
Panthenol (UNII: WV9CM0O67Z)
Sodium Benzoate (UNII: OJ245FE5EU)
Sodium Chloride (UNII: 451W47IQ8X)
Sodium Hydroxide (UNII: 55X04QC32I)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55118-800-63	6 in 1 CARTON	11/16/2018
1	NDC: 55118-800-10	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 55118-800-65	2 in 1 CARTON	11/16/2018
2	NDC: 55118-800-12	1200 mL in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC: 55118-800-66	2 in 1 CARTON	11/16/2018
3	NDC: 55118-800-15	1500 mL in 1 BOTTLE; 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	11/16/2018

Labeler - Kimberly-Clark (830997032)