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Hand Sanitizer by CVS Pharmacy, Inc

Dosage form: gel
Ingredients: ALCOHOL 70mL in 100mL
Labeler: CVS Pharmacy, Inc
NDC Code: 59779-219

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

Active Ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

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

Warnings

For external use only: hands

Flammable

Keep away from fire and 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
  • irritation or redness develops
  • condition persists for more than 72 hours

Keep out of reach of children

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

Directions
  • wet hands thoroghly 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, glyceryl caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, acrylates/C10-30 alkyl acrylate crosspolymer, benzophenone-4, fragence, red 40, yellow 5

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

Distributed by: CVS Pharmacy, Inc
One CVS Drive, /Woonsocket, RI 02895
2015 CVS/pharmacy
CVS.com 1-800-SHOP CVS
Made in the U.S.A. with U.S. and foreign components

Principal Display Panel

tangerine scent

advanced formula hand sanitizer

kills 99.99% of germs

fast & effective

moisturizing formula with vitamin E

leaves hand feeling soft

CVS/pharmacy

8 FL OZ (236 mL)

566.001/566AB

HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-219
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
water 
GLYCERYL CAPRYLATE/CAPRATE 
GLYCERIN 
ISOPROPYL MYRISTATE 
.ALPHA.-TOCOPHEROL ACETATE 
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) 
SULISOBENZONE 
FD&C RED NO. 40 
FD&C YELLOW NO. 5 
Packaging
#Item CodePackage Description
1NDC:59779-219-34236 mL in 1 BOTTLE, PUMP
2NDC:59779-219-1659 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A11/22/2015
Labeler - CVS Pharmacy, Inc (062312574)
Registrant - Vi-Jon (790752542)
Establishment
NameAddressID/FEIOperations
Vi-Jon088520668manufacture(59779-219)

 
CVS Pharmacy, Inc

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Medically reviewed on Nov 15, 2017

Further information

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

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