FENDALL PURE FLOW- purified water liquid

Fendall Pure Flow by

Drug Labeling and Warnings

Fendall 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

Do not use

• 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

• 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

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

Directions

• 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

• store at rom temperature, 59 o to 86 o F (15 o to 30 o C)
• do not freeze

Inactive ingredients

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

Questions?

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

Honeywell Safety Products USA, Inc.

855 S. Mint Street, Charlotte, NC, 28202

Principle Display Panel

INGREDIENTS AND APPEARANCE

FENDALL PURE FLOW 
purified water liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0498-0630
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
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)
SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
EDETATE DISODIUM (UNII: 7FLD91C86K)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0498-0630-37	14.38 L in 1 CONTAINER; Type 0: Not a Combination Product	12/15/2018

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. (198541331)