HAWS EYEWASH ADDITIVE- purified water solution, concentrate

Haws Eyewash Additive by

Drug Labeling and Warnings

Haws Eyewash Additive by is a Otc medication manufactured, distributed, or labeled by Haws Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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)

INGREDIENTS AND APPEARANCE

HAWS EYEWASH ADDITIVE 
purified water solution, concentrate

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66051-210
Route of Administration	TOPICAL, CUTANEOUS, OPHTHALMIC, IRRIGATION

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R)	WATER	889.6 g  in 1000 mL

Inactive Ingredients
Ingredient Name	Strength
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66051-210-50	4 in 1 BOX	07/03/2014
1		148 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	07/03/2014

Labeler - Haws Corporation (009124785)