HEALTHY HANDS  INSTANT ANTISEPTIC HAND CLEANSER- alcohol solution 
NCH Corporation

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.

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Healthy Hands™
Instant Antiseptic Hand Cleanser

Drug Facts

Active ingredient

Ethyl Alcohol (62%)

Purpose

Antiseptic Compound

Uses

Warnings

Flammable liquid and vapor

For external use only

Causes eye irritation

May be harmful if swallowed

Do not use

  • near heat or flame.
  • around the eyes.

Stop use and ask a doctor if irritation and redness develop. If condition persists for more than 72 hours, consult a doctor.

Keep out of reach of children

For eye contact

Rinse eyes with water. Remove any contact lenses and continue flushing with plenty of water for several minutes. Seek medical attention if irritation develops.

If swallowed

Give 3 or 4 glasses of water, but DO NOT induce vomiting. If vomiting occurs, give fluids again. Seek medical attention if discomfort occurs.

Directions

Inactive ingredients

Water, Carbomer, Diisopropylamine, Polysorbate 80, Cetyl Acetate, Acetylated Lanolin Alcohol, Propylene Glycol, Diazolidinyl Urea, Methylparaben, and Propylparaben.

Questions or comments

For medical or environmental emergencies, call CHEMTREC® at 1-800-424-9300.

Manufactured for
MULTI-MIST Products
A Division of NCH Corporation
1618 Northgate, Irving, Texas 75

PRINCIPAL DISPLAY PANEL - 237 ml Bottle Label

Healthy Hands

Instant Antiseptic Hand Cleanser

Read the entire label before using this product.

(See the back panel for warnings.)

multiMIST

Manufactured for
MULTI-MIST Products
A Division of NCH Corporation
1618 Northgate, Irving, Texas 75
©2008 NCH Corporation

QUALITY
ASSURANCE
ISO 9001

TO REORDER, Call TOLL-FREE:
1-800-527-9919
FAX: 972-438-0634

NET CONTENTS: 8 fl oz/237 ml

Principal Display Panel - 237 ml Bottle Label
HEALTHY HANDS   INSTANT ANTISEPTIC HAND CLEANSER
alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55533-522
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL42 mg  in 25 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Diisopropylamine (UNII: BR9JLI40NO)  
Polysorbate 80 (UNII: 6OZP39ZG8H)  
Propylene Glycol (UNII: 6DC9Q167V3)  
Diazolidinyl Urea (UNII: H5RIZ3MPW4)  
Methylparaben (UNII: A2I8C7HI9T)  
Propylparaben (UNII: Z8IX2SC1OH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55533-522-26237 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E11/01/2000
Labeler - NCH Corporation (126655562)

Revised: 12/2012
Document Id: 7a7a7ec5-30b6-418c-80ee-1be515e761e3
Set id: bd38ac39-9f4f-4a50-b688-cbdea95df2a1
Version: 2
Effective Time: 20121211
 
NCH Corporation