Fendall Pure Flow

Manufacturer: Honeywell Safety Products USA, Inc.
Effective date: 2024-12-10
Label type: HUMAN OTC DRUG LABEL
Version: 9
Source: full-release
Hydrated at: 2026-06-01 00:54:30

Label at a glance#

ProductFendall Pure Flow

Active ingredientWATER

Label structure10 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 activation 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 contact800-430-5490

PhoneLabel contact888-212-7233

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

Do not use

OTC - DO NOT USE SECTION

if solution changes color or gets cloud
in open wounds in or near eyes
with contact lenses

Stop use and ask a doctor if you have

OTC - STOP USE SECTION

changes in vision
eye pain
continued redness or irritation of the eyes 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 activation 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

Other information

OTHER SAFETY INFORMATION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Questions?

OTC - QUESTIONS SECTION

USA: 800-430-5490 Canada: 888-212-7233

Honeywell Safety Products USA, Inc.

855 S. Mint Street, Charlotte, NC, 28202

Changes from previous version

RECENT MAJOR CHANGES SECTION

Indications and Usage
Warnings and Precautions

Principle Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

32-005565 Rev. N - NDC 0498-0630-37

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1053173	water 98.6 % Ophthalmic Irrigation Solution	PSN	9
1053173	water 986 MG/ML Ophthalmic Irrigation Solution	SCD	9
1053173	water 98.577 % Ophthalmic Irrigation Solution	SY	9
1053173	water 98.6 % Ophthalmic Irrigation Solution	SY	9
1053173	water 98.6 ML per 100 ML Ophthalmic Irrigation Solution	SY	9

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0498-0630-37	Fendall Pure Flow	14.38 L in 1 CONTAINER	LIQUID	14.38		9

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0498-0630	FENDALL PURE FLOW (PURIFIED WATER) LIQUID [HONEYWELL SAFETY PRODUCTS USA, INC.]	9	Current NDC, Legacy NDC, 1 package rows	20250207_afda6fc3-7615-b0be-e053-2995a90a6208.zip

Products#

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

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0498-0630	0498-0630-37

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

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 Pure Flow	PURIFIED WATER	Honeywell Safety Products USA, Inc.	afda6fc3-7615-b0be-e053-2995a90a6208	2024-12-10	Warnings	Exact identifier ndc (package): 0498-0630-37 ndc (product): 0498-0630 ndc11 (package): 00498063037 spl id: 28eea87a-8088-19aa-e063-6394a90aad4a spl set id: afda6fc3-7615-b0be-e053-2995a90a6208

Reported adverse events (FAERS/openFDA)#

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