SCOTT FOAM HAND SANITIZER- benzalkonium chloride solution

SCOTT FOAM HAND SANITIZER by

Drug Labeling and Warnings

SCOTT FOAM HAND SANITIZER 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 0.13 %

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. Rub thoroughly into hands for at least 30 seconds. Allow to dry.

Inactive ingredients

Aloe Barbadensis Leaf Juice Powder, Citric Acid, Cocamidopropyl PG-Dimonium Chloride Phosphate, Methylpropanediol, Panthenol, Polyethylene Glycol, Silica, Sodium Hydroxide, 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 - 40.5 fl oz Bottle Label

12979

Empty &
Discard Pump
PLASTIC
BOTTLE
how2recycle.info

DIN 02481456

For Personal / Domestic Use Only

Scott®
Brand

Foam Hand Sanitizer

Benzalkonium Chloride Solution, USP

Alcohol free

SAME GREAT
FORMULATION.
Now Scott®
branded!

LEAVE ON

20-14-557-0-05

1.2 L (40.5 fl oz)

INGREDIENTS AND APPEARANCE

SCOTT FOAM HAND SANITIZER 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55118-664
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y)	Benzalkonium Chloride	1.3 mg  in 1000 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CALCIUM (UNII: SY7Q814VUP)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
METHYLPROPANEDIOL (UNII: N8F53B3R4R)
PANTHENOL (UNII: WV9CM0O67Z)
POLYETHYLENE OXIDE 600000 (UNII: 2126FD486L)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
Sodium Hydroxide (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55118-664-63	6 in 1 CARTON	11/16/2018
1	NDC: 55118-664-10	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 55118-664-65	2 in 1 CARTON	11/16/2018
2	NDC: 55118-664-12	1200 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)