EYEWASH STATION ADDITIVE CONCENTRATE- chlorhexidine gluconate and propylene glycol liquid 
Niagara Pharmaceuticals Inc.

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EYEWASH STATION

ADDITIVE

CONCENTRATE

Product Information

Ingredients

Chlorhexidine gluconate 1% w/v Purified Water, Propylene Glycol

Purpose

Preservative

Use

A preservative for use in potable self-contained emergency eyewash stations

Warnings

For external use only. In case of contact with eye in undiluted form, flush with clean water

Do not use

  • in full strength

When using this product

  • do not change dilution or use with other chemicals
  • do not reuse

Stop use and ask a doctor if you have any of the following

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

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Questions ?

☎ Call 905 690-6277 9 a.m. to 5 p.m. EST Mon-Fri

Manufactured by:
Niagara Pharmaceuticals Inc.
60 Innovation Dr.
Flamborough ON L9H 7P3

PRINCIPAL DISPLAY PANEL - 236 mL Bottle Label

EYEWASH STATION
ADDITIVE
CONCENTRATE

NDC 65785-034-01

A preservative for potable water.
Preserves from 5 - 20 US Gallons
(15 - 76 Liters)

FOR USE IN EMERGENCY
EYEWASH STATIONS.

Manufactured by:
Niagara Pharmaceuticals Inc.
60 Innovation Dr.
Flamborough ON L9H 7P3
Made in Canada

8 Fl Oz [236 mL]

HEALTH SAVER®

The Safe Solution™

PRINCIPAL DISPLAY PANEL - 236 mL Bottle Label
EYEWASH STATION ADDITIVE CONCENTRATE 
chlorhexidine gluconate and propylene glycol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65785-034
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE GLUCONATE145.6 kg  in 2800 L
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL280 kg  in 2800 L
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R) 2374.4 L  in 2800 L
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65785-034-010.236 L in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product11/15/2011
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01811/15/2011
Labeler - Niagara Pharmaceuticals Inc. (205477792)
Registrant - Niagara Pharmaceuticals Inc. (205477792)
Establishment
NameAddressID/FEIBusiness Operations
Niagara Pharmaceuticals Inc.205477792manufacture(65785-034)

Revised: 10/2023
Document Id: 06a7aecc-d271-40f4-e063-6294a90a702e
Set id: 362a6b6d-862d-4322-87a8-5b3a07fbe174
Version: 4
Effective Time: 20231001
 
Niagara Pharmaceuticals Inc.