FDA.reportPublic FDA data

Purified Eyesaline Emergency Eyewash (1 gal)

Manufacturer
Honeywell Safety Products USA, Inc.
Effective date
2025-11-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
monthly-update
Hydrated at
2026-07-17 21:36:11

Label at a glance#

ProductEyesaline Emergency Eyewash
Active ingredientWATER
Label structure11 sections

Indications and uses

For flushing or irrigating the eye to reduce chances of severe injury caused by acid, alkali, or particulate contamination

Dosage and administration

remove contacts before using flush the affected area as needed if necessary, continue flushing with emergency eyewash or shower do not reuse keep bottle upright discard cartridge after use

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Purified Water 98.6%

Purpose

OTC - PURPOSE SECTION

Emergency Eyewash

Uses

INDICATIONS & USAGE SECTION

For flushing or irrigating the eye to reduce chances of severe injury caused by acid, alkali, or particulate contamination

Warnings

WARNINGS SECTION

For external use only

  • Obtain Immediate medical treatment for all open wounds in or near the eyes
  • To avoid contamination, do not touch tip of container to any surface.
  • Do not reuse, once opened, discard.

Do not use

OTC - DO NOT USE SECTION

  • If solution changes color or gets cloudy
  • In open wounds in or near the eyes
  • with contact lenses
  • if seal is broken or tampered with
  • if eye is lacerated or object is embedded

Stop use and ask a doctor if you have

OTC - STOP USE SECTION

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

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

  • remove contacts before using
  • flush the affected area as needed
  • if necessary, continue flushing with emergency eyewash or shower
  • do not reuse
  • keep bottle upright
  • discard cartridge after use

Inactive Ingredients

INACTIVE INGREDIENT SECTION

benzalkonium chloride, edetate disodium, sodium chloride, sodium phosphate dibasic, sodium phosphate monobasic

Questions?

OTC - QUESTIONS SECTION

USA: 800-430-5490

Canada: 888-212-7233

Protective Industrial Products, Inc.

25 British American Blvd.

Latham, NY 12110, USA

Label Artwork

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FF Cartridge ArtworkFF Cartridge Artwork1 Gal F Style Artwork1 Gal F Style Artwork

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0498-06210498-0621-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
SODIUM PHOSPHATE, DIBASICGR686LBA74IACT
WATER059QF0KO0RACTIB
EDETATE DISODIUM7FLD91C86KIACT
SODIUM CHLORIDE451W47IQ8XIACT
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE593YOG76RNIACT

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
Eyesaline Emergency EyewashPURIFIED WATERHoneywell Safety Products USA, Inc.37f244fd-c02f-e66a-e063-6394a90aed812025-11-12WarningsExact identifier
ndc (package): 0498-0621-01
ndc (product): 0498-0621
ndc11 (package): 00498062101
spl id: 55072634-c6a3-d426-e063-6294a90a6108
spl set id: 37f244fd-c02f-e66a-e063-6394a90aed81