KLEENEX REVEAL 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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Kleenex® Reveal™ Moisturizing Foam Hand Sanitizer

Drug Facts

Active ingredient

Ethyl Alcohol 70% v/v

Purpose

Antimicrobial

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 immediately.

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

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

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 - 532 mL Bottle Label

Kleenex®
BRAND
MARQUE

REVEAL™

MOISTURIZING FOAM HAND SANITIZER

ULTRA

For Personal / Domestic Use Only
18 fl oz (532 mL)

PRINCIPAL DISPLAY PANEL - 532 mL Bottle Label
KLEENEX REVEAL MOISTURIZING FOAM HAND SANITIZER 
alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55118-531
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)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
Glycerin (UNII: PDC6A3C0OX)  
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:55118-531-6424 in 1 CARTON05/15/2018
1NDC:55118-531-1145 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:55118-531-674 in 1 CARTON05/15/2018
2NDC:55118-531-18532 mL in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:55118-531-106 in 1 CARTON06/01/2022
31000 mL in 1 BOTTLE; Type 0: Not a Combination Product
4NDC:55118-531-122 in 1 CARTON06/01/2022
41200 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 finalpart333E05/15/2018
Labeler - Kimberly-Clark (830997032)

Revised: 7/2023
Document Id: d2bf8c39-22f8-4b53-a4ed-299d89e0365f
Set id: 4a491f90-268e-470d-a74c-473f1efe7c8b
Version: 5
Effective Time: 20230712
 
Kimberly-Clark