Fendall 2000 Pure Flow

Manufacturer: Honeywell Safety Products USA, Inc. | Keystone Industries
Effective date: 2024-01-06
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: full-release
Hydrated at: 2026-06-01 00:06:47

Label at a glance#

ProductFendall 2000 Pure Flow

Active ingredientWATER

Label structure8 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 do not reuse discard cartridge after use

Contacts and useful links#

PhoneLabel contact1-800-430-5490

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

store at room temperature, 59 ^oto 86 ^oF (15 ^o to 30 ^oC)
do not freeze

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

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

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
do not reuse
discard cartridge after use

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Questions?

OTC - QUESTIONS SECTION

Call 1-800-430-5490

Sperian Eye & Face Protecton, Inc.

(a Honeywell Company)

825 East Highway 151

Platteville, WI 53818 USA

Principle Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Fendall 2000Fendall 2000 PI

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1053173	water 98.6 % Ophthalmic Irrigation Solution	PSN	5
1053173	water 986 MG/ML Ophthalmic Irrigation Solution	SCD	5
1053173	water 98.577 % Ophthalmic Irrigation Solution	SY	5
1053173	water 98.6 % Ophthalmic Irrigation Solution	SY	5
1053173	water 98.6 ML per 100 ML Ophthalmic Irrigation Solution	SY	5

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
726062af-1135-4707-a1d7-57256991bbf9	Product name	2	20250226
19c71a3d-ed9c-166b-a7e5-38c250c35631	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
0498-0631-37	2024-01-06	C162847	48780-1	0191ceaa-69c6-198a-e063-dbdaa90aec3e	0498-0631: Fendall 2000 Pure flow
0498-0631-37	2023-07-28	C162847	48780-1	0191ceaa-69c6-198a-e063-dbdaa90aec3e	0498-0631: Fendall 2000 Pure flow

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0498-0631-37	Fendall 2000 Pure Flow	29.9 L in 1 CONTAINER	LIQUID	29.9		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0498-0631	FENDALL 2000 PURE FLOW (PURIFIED WATER) LIQUID [HONEYWELL SAFETY PRODUCTS USA, INC.]	5	Current NDC, Legacy NDC, 1 package rows	20240107_b56ef662-fec2-4d94-e053-2995a90aba2b.zip

Products#

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

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

Fendall 2000 Pure Flow
Purified water
EDETATE DISODIUM
BENZALKONIUM CHLORIDE
SODIUM CHLORIDE
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
SODIUM PHOSPHATE, DIBASIC
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0498-0631	0498-0631-37

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
Name	UNII	Kind
EDETATE DISODIUM	7FLD91C86K	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE	593YOG76RN	IACT
SODIUM PHOSPHATE, DIBASIC	GR686LBA74	IACT
WATER	059QF0KO0R	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Fendall 2000 Pure Flow	PURIFIED WATER	Honeywell Safety Products USA, Inc.	b56ef662-fec2-4d94-e053-2995a90aba2b	2024-01-06	Warnings	Exact identifier ndc (package): 0498-0631-37 ndc (product): 0498-0631 ndc11 (package): 00498063137 spl id: 0e4a17cb-beaf-6525-e063-6394a90a16b0 spl set id: b56ef662-fec2-4d94-e053-2995a90aba2b

Reported adverse events (FAERS/openFDA)#

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