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Advanced Hand Sanitizer by DZA Brands

Medically reviewed on Dec 8, 2017

Dosage form: gel
Ingredients: ALCOHOL 700mg in 1mL
Labeler: DZA Brands
NDC Code: 55316-439

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.

Advanced Hand Sanitizer with Aloe

Active ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Uses
  • to decrease bacteria on the skin that could cause disease
  • recommended for repeated use

Warnings

For external use only-hands

Flammable.  Keep away from fire or flame.

When using this product
  • keep out of eyes.  In case of contact with eyes, flush thoroughly with water.
  • avoid contact with broken skin
  • do not inhale or ingest

Stop use and ask a doctor if

skin irritation develops

Keep out of reach of children.

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

Directions
  • wet hands thoroughly with product and allow to dry without wiping
  • for children under 6, use only under adult supervision
  • not recommended for infants

Other information
  • do not store above 105⁰ F
  • may discolor some fabrics
  • harmful to wood finishes and plastics

Inactive ingredients

water, aloe barbadensis leaf juice, glyceryl caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, benzophenone-4, blue 1, yellow 5

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

Distributed by:
DZA Brands, LLC

Salisbury, NC 28147/Scorbourogh, ME 04074

For product questions or concerns, contact us at 1-866-322-2439. please include UPC number and code from package.

Patent pending

Principal display panel

Healthy accents

Hand sanitizer with aloe

Advanced

more-effective formula

Compare to Purell*

8 FL OZ (236 mL)

439.000/439AB

ADVANCED HAND SANITIZER 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55316-439
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL700 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
ALOE VERA LEAF 
GLYCERYL CAPRYLATE/CAPRATE 
GLYCERIN 
ISOPROPYL MYRISTATE 
.ALPHA.-TOCOPHEROL ACETATE 
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) 
SULISOBENZONE 
FD&C BLUE NO. 1 
FD&C YELLOW NO. 5 
Packaging
#Item CodePackage Description
1NDC:55316-439-34236 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/27/2014
Labeler - DZA Brands (090322194)
Registrant - Vi-Jon, Inc. (790752542)
Establishment
NameAddressID/FEIOperations
Vi-Jon, Inc.088520668manufacture(55316-439)

 
DZA Brands

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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