EYEWASH- water solution 
Akorn

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Drug Facts

Active ingredient

Purified water 98.3%

Purpose

Eyewash

Use

For cleansing the eye to help relieve irritation or burning by removing loose foreign material

Warnings

For external use only

Do not use

  • if you experience any open wounds in or near the eyes and obtain immediate medical treatment
  • if solution changes color or becomes cloudy

When using this product

  • to avoid contamination, do not touch tip of container to any surface
  • do not reuse
  • once opened, discard

Stop use and ask a doctor if you experience

  • 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

Flush the affected eye as needed, controlling the rate of flow of solution by pressure on the bottle.

Other information

Inactive ingredients

boric acid, sodium borate, sodium chloride

Questions ?

Call 888-628-0581

Principal Display Panel Text for Container Label:

Akorn logo

OPHTHALMIC

SOLUTION

EYEWASH

Purified Water, 98.3%

NDC 59399-001-04

Single Use

FOR ANIMAL USE ONLY

Distributed by:

Akorn Operating Company LLC

Gurnee, IL

60031

EVAAL Rev. 07/22

Made in

Canada

Sterile

Solution

4 fl.oz. (118 mL)

Principal Display Panel Text for Container Label
EYEWASH 
water solution
Product Information
Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:59399-001
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Water (UNII: 059QF0KO0R) (Water - UNII:059QF0KO0R) Water929 g  in 946 mL
Inactive Ingredients
Ingredient NameStrength
Boric Acid (UNII: R57ZHV85D4)  
Sodium Borate (UNII: 91MBZ8H3QO)  
Sodium Chloride (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59399-001-041 in 1 BOTTLE
1118 mL in 1 BOTTLE
2NDC:59399-001-081 in 1 BOTTLE
2236 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Unapproved drug other02/01/2015
Labeler - Akorn (117693100)

Revised: 7/2022
Document Id: 5c2ebd8a-de96-474c-b551-043cc265b815
Set id: 6dc20e8a-cf22-43fd-af73-034e5e045b42
Version: 5
Effective Time: 20220712
 
Akorn