FDA.reportPublic FDA data

Eyewash Additive Concentrate

Manufacturer
Haws Corporation | Niagara Pharmaceuticals Inc.
Effective date
2025-11-20
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:17:26

Label at a glance#

ProductEyewash Additive Concentrate
Active ingredientWATER, PROPYLENE GLYCOL
Label structure9 sections

Dosage and administration

wear protective eyewear and gloves clean potable eyewash station and rinse with potable water partially fill station with potable water remove tamper evident seal and cap of bottle add entire contents of the bottle to the eyewash station container fill the station to the manufacturer’s required level date and initial inspection tag station should be cleaned and refilled every 120 days when using this product in ad...

Storage and handling

lot number is printed on the bottle store at 20° to 25° C [68° to 77° F] for your protection, this bottle has an imprinted white seal with black printing "TAMPER EVIDENT SEAL" do not use if this seal is missing or broken use before expiration date marked on bottle

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Propylene Glycol, Water

Purpose

OTC - PURPOSE SECTION

Antimicrobial Preservative

Use

INDICATIONS & USAGE SECTION

A preservative for use in potable self-contained emergency eyewash stations

Warnings

WARNINGS SECTION

For external use only.In case of contact with eye in undiluted form, flush with clean water

Do not use

OTC - DO NOT USE SECTION

  • In full strength

When using this product

OTC - WHEN USING SECTION

  • do not change dilution or use with other chemicals
  • do not reuse

Stop use and ask a doctor if you have any of the following

OTC - ASK DOCTOR SECTION

  • changes in vision
  • eye pain
  • condition worsens or persists
  • continued redness or irritation of the eye

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • wear protective eyewear and gloves
  • clean potable eyewash station and rinse with potable water
  • partially fill station with potable water
  • remove tamper evident seal and cap of bottle
  • add entire contents of the bottle to the eyewash station container
  • fill the station to the manufacturer’s required level
  • date and initial inspection tag
  • station should be cleaned and refilled every 120 days when using this product
  • in advance of emergency, add the concentrate to potable water to have a solution available

Inactive ingredient

INACTIVE INGREDIENT SECTION

Chlorhexidine gluconate

Other information

STORAGE AND HANDLING SECTION

  • lot number is printed on the bottle
  • store at 20° to 25° C [68° to 77° F]
  • for your protection, this bottle has an imprinted white seal with black printing "TAMPER EVIDENT SEAL"
  • do not use if this seal is missing or broken
  • use before expiration date marked on bottle

Questions ?

OTC - QUESTIONS SECTION

☎ Call 888-640-4297 or 775-359-4712 6 a.m. to 4.30 p.m. PST Monday-Friday

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HAWS

NDC 66051-236-80

EYEWASH ADDITIVE CONCENTRATE

Algaecide, Bactericide, Fungicide

Antimicrobial preservative for a self-contained, emergency eyewash station.

Preserves from 5 - 20 US Gallons
(18.9 - 75.7 Liters)

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

Model 9082

Made in Canada

8 Fl Oz [236 mL]

LabelLabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
bb6d6c68-649d-4e6d-a1f6-603d969c8f68Product name120160303

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66051-236-80Eyewash Additive Concentrate0.236 L in 1 BOTTLE, UNIT-DOSELIQUID0.2364

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66051-23666051-236-80

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
CHLORHEXIDINE GLUCONATEMOR84MUD8EIACT
WATER059QF0KO0RACTIB
PROPYLENE GLYCOL6DC9Q167V3ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Eyewash Additive ConcentrateWATER AND PROPYLENE GLYCOLHaws Corporationdd168403-398c-41ff-b1df-d93e4ff39de32025-11-20WarningsExact identifier
ndc (package): 66051-236-80
ndc (product): 66051-236
ndc11 (package): 66051023680
spl id: 44085c67-0036-59d4-e063-6294a90a46f1
spl set id: dd168403-398c-41ff-b1df-d93e4ff39de3

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.