FDA.reportPublic FDA data

Fendall 2000

Manufacturer
Honeywell Safety Products USA, Inc.
Effective date
2026-06-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
monthly-update
Hydrated at
2026-07-17 21:36:02

Label at a glance#

ProductFendall 2000 Pure Flow
Active ingredientWATER
Label structure12 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

pull handle on the activating door to initiate flow lower head into flow for 15 minutes if necessary, continue flushing with emergency eyewash or shower

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Purified Water 98.66%

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.

OTC - DO NOT USE SECTION

  • If solution changes color or gets cloudy
  • In open wounds in or near the eyes
  • with contact lenses

Stop use and ask a doctor if

OTC - STOP USE SECTION

Stop use and ask a doctor if

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • pull handle on the activating door to initiate flow
  • lower head into flow for 15 minutes
  • if necessary, continue flushing with emergency eyewash or shower

Other information

OTHER SAFETY INFORMATION

Other information

  • Store at room temperature, 59º to 86ºF (15º to 30ºC)
  • Do not freeze

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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

Questions

OTC - QUESTIONS SECTION

Call 800-430-5490

Protective Industrial Products, Inc.

25 British American Blvd.

Latham, NY 12110, USA

Label Artwork

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Fendall 2000 artworkFendall 2000 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
0498-06330498-0633-01

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
WATER059QF0KO0RACTIB
EDETATE DISODIUM7FLD91C86KIACT
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE593YOG76RNIACT
SODIUM PHOSPHATE, DIBASICGR686LBA74IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
SODIUM CHLORIDE451W47IQ8XIACT

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
Fendall 2000 Pure FlowPURIFIED WATERHoneywell Safety Products USA, Inc.37dead3e-60cb-88ae-e063-6294a90a8f702026-06-24WarningsExact identifier
ndc (package): 0498-0633-01
ndc (product): 0498-0633
ndc11 (package): 00498063301
spl id: 550168af-0ce3-f5ee-e063-6394a90a960d
spl set id: 37dead3e-60cb-88ae-e063-6294a90a8f70

Reported adverse events (FAERS/openFDA)#

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