Skip to Content

← See all Hand Sanitizer brands

Hand Sanitizer by McKesson

Medically reviewed on May 29, 2018

Dosage form: gel
Ingredients: ALCOHOL 65.0mL in 100L
Labeler: McKesson
NDC Code: 49348-982

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.

Drug Facts

Active Ingredient
Ethyl Alcohol 65%

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 heat and flame.

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

Stop use and ask a doctor if skin irritation develops.

Keep out of reach of children.  In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

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 about 105⁰ • may discolor some fabrics •harmful to wood finishes and plastics

Inactive ingredients aloe barbadensis leaf juice, benzophenone-4, blue 1, carbomer, fragrance, glycerin, isopropyl myristate, propylene glycol, tocopheryl acetate, water, yellow 5.

Effective at eliminating over 99.99% of many common harmful germs and bacteria in as little as 15 seconds.
Made in USA with US and foreign components.
Not manufactured or distributed by Johnson and Johnson, the owner and distributor of Purell Hand Sanitizer

Sunmark
Compare to
Purell
NDC 49348-982-37
Hand
Sanitizer
Kills germs
without water
WITH ALOE
8 FL OZ (236 mL)
HAND SANITIZER 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49348-982
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL65.0 mL  in 100 L
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF 
SULISOBENZONE 
FD&C BLUE NO. 1 
CARBOMER INTERPOLYMER TYPE A (55000 MPA.S) 
GLYCERIN 
ISOPROPYL MYRISTATE 
PROPYLENE GLYCOL 
.ALPHA.-TOCOPHEROL ACETATE 
WATER 
FD&C YELLOW NO. 5 
Packaging
#Item CodePackage Description
1NDC:49348-982-37.236 L in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A08/02/2011
Labeler - McKesson (177667227)
Registrant - Vi-Jon (088520668)
Establishment
NameAddressID/FEIOperations
Vi-Jon088520668manufacture

 
McKesson

← See all Hand Sanitizer brands

Further information

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

Hide