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Handi Sani by Vi-Jon

Dosage form: liquid
Ingredients: ALCOHOL 62mL in 100L
Labeler: Vi-Jon
NDC Code: 11344-817

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 ingredients
Ethyl Alcohol 62%

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 heat 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 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 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 benzophenone-4, blue 1, carbomer, fragrance, glycerin, isopropyl alcohol, isopropyl myristate, propylene glycol, red 4,  red 33, tocopheryl acetate, water

Distributed By: Vi-Jon
8515 Page Ave
St. Louis, MO 63114

Handi Sani
Hand Sanitizer
Germ-X
2 FL (59 mL)
HANDI SANI 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11344-817
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL62 mL  in 100 L
Inactive Ingredients
Ingredient NameStrength
SULISOBENZONE 
FD&C BLUE NO. 1 
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) 
GLYCERIN 
ISOPROPYL ALCOHOL 
ISOPROPYL MYRISTATE 
PROPYLENE GLYCOL 
FD&C RED NO. 4 
D&C RED NO. 33 
ALPHA-TOCOPHEROL ACETATE 
WATER 
Packaging
#Item CodePackage Description
1NDC:11344-817-16.059 L in 1 BOTTLE, PLASTIC
2NDC:11344-817-18.073 L in 1 BOTTLE, PLASTIC
3NDC:11344-817-21.089 L in 1 BOTTLE, PLASTIC
4NDC:11344-817-34.236 L in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A04/02/2012
Labeler - Vi-Jon (150931459)
Registrant - Vi-Jon (790752542)
Establishment
NameAddressID/FEIOperations
Vi-Jon088520668manufacture

Revised: 04/2012
Document Id: 257aa52e-8d97-490d-a7bc-a07ac8c3f027
Set id: 4ee0e547-b848-462a-a30e-10be6f4720cc
Version: 1
Effective Time: 20120402
 
Vi-Jon

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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 drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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