SCOTT MOISTURIZING FOAM HAND SANITIZER- alcohol solution 
Kimberly-Clark

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Scott® Moisturizing Foam Hand Sanitizer

Drug Facts

Active ingredient

Ethyl Alcohol 62% v/v

Purpose

Antiseptic cleanser

Uses

For personal hand hygiene to help prevent the spread of bacteria. Kills harmful bacteria or germs.

Warnings

For external use only

Flammability warning

Keep away from open flame and sources of heat.

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

Stop use and ask a doctor if

irritation or redness develops or persists.

Keep out of reach of children. If swallowed, get medical help or contact a poison control centre right away.

Directions

Use enough foam to cover your hands. Supervise children when they use this product. For occasional and personal domestic use. Rub thoroughly into hands for at least 30 seconds. Allow to dry. Use as part of your daily cleansing routine.

Other information

Report serious side effects from this product to 1-877-561-6587. Do not store above 110 °F (40 °C).

Inactive ingredients

Betaine, Fragrance, Meadowfoam Amidopropyl Betaine, PEG-10 Dimethicone, PEG-7 Gylceryl Cocoate, Water

Questions?

1-888-346-4652

Manufactured Distributed in the U.S. by Kimberly-Clark Global Sales, LLC, Roswell, GA 30076-2199
Distributed in Canada by Kimberly-Clark Inc., Mississauga, Ontario L5B 3Y5

PRINCIPAL DISPLAY PANEL - 1.2 Liter Bottle Label

91590

Empty &
Discard Pump

PLASTIC
BOTTLE

how2recycle.info

Scott®
Brand

Moisturizing Foam Hand Sanitizer

NPN: 80015523
For Personal / Domestic Use Only

LEAVE ON

20-14-830-0-01

1.2 Liters (40.5 fl oz)

PRINCIPAL DISPLAY PANEL - 1.2 Liter Bottle Label
SCOTT MOISTURIZING FOAM HAND SANITIZER 
alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55118-546
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol62 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Betaine (UNII: 3SCV180C9W)  
Meadowfoamamidopropyl Betaine (UNII: HNV0L650LG)  
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)  
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55118-546-636 in 1 CARTON04/16/2018
1NDC:55118-546-101000 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:55118-546-652 in 1 CARTON04/16/2018
2NDC:55118-546-121200 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E04/16/2018
Labeler - Kimberly-Clark (830997032)

Revised: 7/2023
Document Id: 32a4ad5e-18bf-43c0-a938-f0afb3e3b5c5
Set id: 25900e62-c8fd-4942-ad38-4b9924308460
Version: 6
Effective Time: 20230713
 
Kimberly-Clark