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Haws Eyewash Additive

Dosage form: solution, concentrate
Ingredients: WATER 889.6g in 1000mL
Labeler: Haws Corporation
NDC Code: 66051-210

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

Purified water 88.96% w/v

Purpose

Antimicrobial Preservative

Use

To preserve potable water in 5-20 gallons (18.93L-75.7L) self-contained emergency eyewash stations.

Warnings

Do not use

full strength in the eyes
internally
if twist-off top is broken or missing
mix with other chemicals or eyewash solutions

When using this product

to avoid contamination, do not touch tip of container to any surface
use only as directed
use before expiration date
once opened, discard

 

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions
clean portable self-contained station
rinse with potable water
partially fill station with potable water
add entire contents of this bottle
fill tank completely with potable water
date station’s inspection tag
change solution at least every 90 days or earlier if used
use good judgment based upon the station’s environmental exposure to determine when scheduled solution changes should occur
in advance of an emergency

Other information
testing: follow station’s instructions for use
store 2-40°C (36-104°F)
use 15-30°C (59-86°F)

Inactive ingredients

Propylene glycol, Chlorhexidine gluconate

Questions?

1-888-640-4297 + 1-775-359-4712. Hours 6am – 4:30pm PST Monday – Thursday and 6am – 4:00pm PST Friday

Package/Label Principal Display Panel

Haws

EYEWASH ADDITIVE CONCENTRATE

Algaecide, Bactericide, Fungicide

Sterile antimicrobial preservative for a self-contained, emergency eyewash station.

Manufactured for
Haws Corporation Sparks NV 89431
www.hawsco.com

Model 9082

Made in Singapore

5 fl. oz. (148 mL)

HAWS EYEWASH ADDITIVE 
purified water solution, concentrate
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66051-210
Route of AdministrationTOPICAL, CUTANEOUS, OPHTHALMIC, IRRIGATIONDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WATER (WATER) WATER889.6 g  in 1000 mL
Inactive Ingredients
Ingredient NameStrength
CHLORHEXIDINE GLUCONATE 
PROPYLENE GLYCOL 
Packaging
#Item CodePackage Description
1NDC:66051-210-504 BOTTLE, PLASTIC in 1 BOX
1148 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34907/03/2014
Labeler - Haws Corporation (009124785)

Revised: 06/2014
 
Haws Corporation

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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