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Waterless Hand Sanitizer by Onpoinr, Inc

Medically reviewed on March 12, 2018

Dosage form: gel
Ingredients: ALCOHOL .65mL in 100L
Labeler: Onpoinr, Inc
NDC Code: 51143-203

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

Use •to decrease bacteria on the skin that could cause disease
•recommended for reported 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.  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  •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

Not manufactured or distributed by GOJO Industries,
owner of the registered trademark Purell

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

Distributed by: Onpoint, Inc
2 Paragon Drive,
Montvale, NJ 07645

Live Better
Waterless
Hand
Sanitizer
With Aloe
•Kills 99.99% of Germs
8 FL OZ (236 mL)
WATERLESS HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51143-203
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL.65 mL  in 100 L
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF 
SULISOBENZONE 
FD&C BLUE NO. 1 
GLYCERIN 
ISOPROPYL MYRISTATE 
PROPYLENE GLYCOL 
ALPHA-TOCOPHEROL ACETATE 
WATER 
FD&C YELLOW NO. 5 
Packaging
#Item CodePackage Description
1NDC:51143-203-34.236 L in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A08/01/2011
Labeler - Onpoinr, Inc (001367366)
Registrant - Vi-Jon (088520668)
Establishment
NameAddressID/FEIOperations
Vi-Jon088520668manufacture

 
Onpoinr, Inc

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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