PURIFIED WATER- purified water solution/ drops 
OCuSOFT, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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OCuSOFT® EYE WASH

Active ingredient

Purified Water

Purpose

Eye Wash

Uses

● in an emergency, to help flush loose foreign material or chemicals from the eye.
● to help relieve eye irriatation, burning, itching and stinging by removing air pollutants (smog or pollen) or chlorinated   water.

Warnings 

For external use only

Do not use

● if solution changes colors or becomes cloudy.

When using this product

● remove contact lenses before using.
● avoid contamination do not touch tip of container to any surface. 
● replace cap after using.
● overuse may cause more eye redness.

Stop use and ask a doctor if

● you experience eye pain.
● changes in vision occur.
● continued redness or irritation of the eye.
● condition worsens or persists for more than 72 hours.
● you experience any chemical burns.
● you experience any open wounds in or near the eyes. 

Keep this and all drugs out of the 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

● store at room temperature 15°-30°C (59°-86°F).

Inactive ingredients

Benzalkonium Chloride, Edetate Disodium, Potassium Chloride, Sodium Choride, Sodium Phosphate Dibasic, Sodium Phosphate Monobasic.

Questions or comments?

Call 800-233-5469   www. ocusoft.com

Principal Label Display

Eye Wash

PURIFIED WATER 
purified water solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54799-565
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Water (UNII: 059QF0KO0R) (Water - UNII:059QF0KO0R) Water99.03 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Benzalkonium Chloride (UNII: F5UM2KM3W7)  
Edetate Disodium (UNII: 7FLD91C86K)  
Potassium Chloride (UNII: 660YQ98I10)  
Sodium Chloride (UNII: 451W47IQ8X)  
Sodium Phosphate, Dibasic, Anhydrous (UNII: 22ADO53M6F)  
Sodium Phosphate, Monobasic (UNII: 3980JIH2SW)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54799-565-59118 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product01/01/200905/31/2021
2NDC:54799-565-0130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product01/01/200905/31/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34901/01/200905/31/2022
Labeler - OCuSOFT, Inc. (174939207)

Revised: 10/2021
 
OCuSOFT, Inc.