SCOTT MOISTURIZING FOAM HAND SANITIZER (ULTRA)- 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 (Ultra)

Drug Facts

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose

Antimicrobial

Use

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

Warnings

Flammable - Keep away from open flame and sources of heat.

For External Use Only.

When using this product avoid contact with eyes; in case of contact, flush eyes with water.

Stop use & ask a health care practitioner if irritation or redness develops or persists.

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

Directions

Use enough foam to cover your hands. Rub hands together briskly until dry. Use as part of your daily cleansing routine.

Other Information

Inactive Ingredients

Aloe Barbadensis Leaf Extract, Betaine, Camellia Sinensis Leaf Extract, Citric Acid, Cucumis Sativus (Cucumber) Fruit Extract, Glycerin, Isopropanol, Meadowfoamamidopropyl Betaine, Panthenol, PEG-10 Dimethicone, Water/Eau

Questions?

1-888-346-4652

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 - 33.8 fl oz Bottle Label

34700

SAME GREAT
FORMULATION.
Now Scott®
branded!

Scott®
Brand

Moisturizing
Foam Hand Sanitizer

ULTRA
Leave On

Empty &
Discard Pump
PLASTIC
BOTTLE

20-14-658-0-03

how2recycle.info

ECOLOGO
PRODUCT CERTIFIED FOR
REDUCED ENVIRONMENTAL
IMPACT. VIEW SPECIFIC
ATTRIBUTES EVAUATED:
UL.COM/EL UL 2783

NPN: 80030706

For Personal / Domestic Use Only

1 Liter (33.8 fl oz)

Principal Display Panel - 33.8 fl oz Bottle Label
SCOTT MOISTURIZING FOAM HAND SANITIZER (ULTRA) 
alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55118-532
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Betaine (UNII: 3SCV180C9W)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
CUCUMBER (UNII: YY7C30VXJT)  
Glycerin (UNII: PDC6A3C0OX)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
MEADOWFOAMAMIDOPROPYL BETAINE (UNII: HNV0L650LG)  
Panthenol (UNII: WV9CM0O67Z)  
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)  
Water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55118-532-636 in 1 CARTON04/25/2018
1NDC:55118-532-101000 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:55118-532-652 in 1 CARTON04/25/2018
2NDC:55118-532-121200 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 finalpart333E04/25/2018
Labeler - Kimberly-Clark (830997032)

Revised: 10/2019
Document Id: c9712f1c-bcd6-4e39-a19a-82bfffcd4721
Set id: 6658934b-a1f0-4931-a528-15cee3a91fa7
Version: 2
Effective Time: 20191018
 
Kimberly-Clark