HAND SANITIZER- alcohol gel 
Drug Mart

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
370.001/370AE rev 1

Active Ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Uses

Warnings

For external use only-hands

Flammable.  Keep away from heat and 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

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

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

DISTRIBUTED BY: Discount Drug mart

211 commerce Drive, Medina, Ohio 44256

Made in the USA with US and foreign components

Patent pending

Principal display panel

Discount Drug Mart Food Fair

COMPARE TO PURELL ACTIVE INGREDIENT**

Advanced Hand Sanitizer

More effective formula

Kills more than 99.99% of germs*

8 FL OZ (236 mL)

image description

HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53943-370
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:53943-370-1659 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/21/2012
2NDC:53943-370-34236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/21/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A09/21/2012
Labeler - Drug Mart (047741335)
Registrant - Vi-Jon, LLC (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC088520668manufacture(53943-370)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC790752542manufacture(53943-370)

Revised: 7/2023
Document Id: 11d02eb4-fcd6-422a-b861-978b09f19262
Set id: 741a3b92-5566-4c4b-b37a-1a551fd1e007
Version: 10
Effective Time: 20230705
 
Drug Mart