APPEAL ALCOHOL FOAMING HAND SANITIZER- ethyl alcohol liquid 
SC Johnson Professional USA, Inc.

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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Drug Facts

Active ingredient

Ethyl Alcohol 70% ww

Purpose

Antibacterial

Uses

For hand sanitizing to reduce bacteria on the skin

Warnings

For external use only

Flammable: Keep away from fire or flame.

When using this product avoid contact with eyes.  In case of eye contact, flush with water.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Apply one shot of foaming sanitizer to dry hands

Rub into skin

No rinsing required

Inactive ingredients

Water, Bis-PEG-12 Dimethicone, Behentrimonium Chloride, PEG-200 Hydrogenated Glyceryl Palmate, PEG-7 Glyceryl Cocoate, Coco-Glucoside, Glyceryl Oleate, Dihydroxypropyl PEG-5 Linoleammonium Chlroide

container label

APP17102

102668

appeal Alcohol Foaming Hand Sanitizer

Certified EcoLogo

Certified Instant Hand Antiseptic CCD-170

1 Liter

33.8 Fluid Ounces

Made in Canada by Deb

deb foam technolody

Distributed exclusively by:

Interline Brands

Jacksonville, FL  32207

www.AppealProducts.com

Rev. 05-12

01830

container label

container label

APPEAL ALCOHOL FOAMING HAND SANITIZER 
ethyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-702
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
WATER (UNII: 059QF0KO0R)  
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)  
BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
COCO GLUCOSIDE (UNII: ICS790225B)  
PEG-200 DILAURATE (UNII: TWV5J70L88)  
GLYCERYL COCOATE (UNII: WVK1CT5994)  
GLYCERYL MONOOLEATE (UNII: C4YAD5F5G6)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11084-702-271000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/15/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/15/2012
Labeler - SC Johnson Professional USA, Inc. (607378015)
Establishment
NameAddressID/FEIBusiness Operations
SC Johnson Professional CA Inc.203765300manufacture(11084-702)

Revised: 12/2020
Document Id: 9dedfc3e-92be-447b-b627-f4855dd662f2
Set id: 6b35e9f7-1e3e-41c6-9250-e1ce744b302e
Version: 6
Effective Time: 20201211
 
SC Johnson Professional USA, Inc.