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Hand Sanitizer by Medline Industries, Inc.

Medically reviewed on April 6, 2018

Dosage form: liquid
Ingredients: ALCOHOL 0.879mg in 1mL
Labeler: Medline Industries, Inc.
NDC Code: 53329-209

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.

Hand Sanitizer

Active ingredient

Ethyl alcohol 70% v/v

purpose

Antiseptic

Use
  • 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
  • irritation or redness develops
  • condition persists for more than 72 hours

Keep out of reach 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 suervision
  • not recommended for infants

Other information
  • do not store above 105° F
  • may discolor some fabrics
  • harmful to wood finishes and plastics

inactive ingredients

water, PEG-8 dimethicone, meadowfoamamidopropyl betaine, glyceryl caprylate/caprate, glycerin, tocopheryl acetate, isopropyl myristate

Permits

SDS-MO-15036, SDA WI-2059, WI-2486,

DSP-MO-28, DSP-MO-34, PAT. 9,161,982

Adverse Reactions Section

www.medline.com  2017 Medline Industries, Inc.  Made in USA with US and Foreign components for Medline Industries, Inc., Mundelein, IL

60060 USA.  1-800-MEDLINE

456.001/456AC

Principal Display Panel

MEDLINE

NDC 53329-209-98

SPECTRUM

HAND SANITIZER FOAM

70% ETHYL

ALCOHOL

Added moisturizers

help reduce dry skin

33.8 FL OZ

(1000 mL)

HAND SANITIZER 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53329-209
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL0.879 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
PEG-8 DIMETHICONE 
MEADOWFOAMAMIDOPROPYL BETAINE 
GLYCERYL CAPRYLATE/CAPRATE 
GLYCERIN 
.ALPHA.-TOCOPHEROL ACETATE 
ISOPROPYL MYRISTATE 
Packaging
#Item CodePackage Description
1NDC:53329-209-981000 mL in 1 BOTTLE, PUMP
2NDC:53329-209-80532 mL in 1 BOTTLE, PUMP
3NDC:53329-209-37221 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/27/2016
Labeler - Medline Industries, Inc. (025460908)
Registrant - Vi-Jon, Inc (790752542)
Establishment
NameAddressID/FEIOperations
Vi-Jon, Inc088520668manufacture(53329-209)

 
Medline Industries, 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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