FENDALL 2000 PURE FLOW- purified water liquid

Fendall 2000 Pure Flow by

Drug Labeling and Warnings

Fendall 2000 Pure Flow by is a Otc medication manufactured, distributed, or labeled by Honeywell Safety Products USA, Inc., Sperian. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Purified Water 98.6%

Purpose

Emergency Eyewash

Uses

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

Warnings

For external use only

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

Do not use

• 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

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

Keep out of reach of children

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

Directions

• 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

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

Questions?

Call 1-800-430-5490

Sperian Eye & Face Protecton, Inc.

(a Honeywell Company)

825 East Highway 151

Platteville, WI 53818 USA

Principle Display Panel

INGREDIENTS AND APPEARANCE

FENDALL 2000 PURE FLOW 
purified water liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0498-0631
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R)	WATER	98.6 L  in 100 L

Inactive Ingredients
Ingredient Name	Strength
EDETATE DISODIUM (UNII: 7FLD91C86K)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)
SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0498-0631-37	29.9 L in 1 CONTAINER; Type 0: Not a Combination Product	12/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M018	12/15/2018

Labeler - Honeywell Safety Products USA, Inc. (118768815)

Establishment
Name	Address	ID/FEI	Business Operations
Keystone Industries		014769301	manufacture(0498-0631)