ADVANCED HAND SANITIZER- alcohol gel 
CDMA

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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Advanced Hand Sanitizer
370.001/370AB & AE rev 1

Active Ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Uses

Warnings

For external use only: hands

Flammable.  Keep away from fire or flame.

When using this product

Stop use and ask a doctor if

Keep out of reach of children.

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

Directions

Other information

Inactive ingredients

water, glyceryl caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, benzophenone-4

*This product is not manufactured or distributed by GOJO Industries, Inc, distributer of Purell Advanced Hand Sanitizer.

**Effective at eliminating more than 99.99% of many common harmful germs and bacteria in as little as 15 seconds*

Distributed by CDMA, Inc.

43157 W Nine Mile

Novi, MI 48357

www.qualitychoice.com

Questions: 800-935-2362

principal display panel

QC

Quality Choice

*Compare to Purell Advanced Hand Sanitizer

Advanced Hand Sanitizer

Original

Kills More Than 99.99% of Germs**

Leaves hands feeling soft

With Moisturizers & Vitamin E

2 FL OZ (59 mL)

image description

ADVANCED HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-882
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)  
GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
CARBOMER COPOLYMER TYPE b (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)  
SULISOBENZONE (UNII: 1W6L629B4K)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63868-882-1659 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/05/2021
2NDC:63868-882-34236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/05/2021
3NDC:63868-882-45946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/05/2021
4NDC:63868-882-43473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/05/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A10/05/2021
Labeler - CDMA (011920774)
Registrant - Vi-Jon, LLC (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC088520668manufacture(63868-882)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC790752542manufacture(63868-882)

Revised: 1/2023
Document Id: e539cbae-4bc9-48e3-94f5-d5be15400693
Set id: a85d93f2-e6f0-4fad-9ff7-6cbb62942bb2
Version: 5
Effective Time: 20230131
 
CDMA