Label: MEDICS CHOICE SOOTHING EYE WASH- purified water solution

  • NDC Code(s): 55651-555-01
  • Packager: KC Pharmaceuticals, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 19, 2025

If you are a consumer or patient please visit this version.

View All Sections
  • Active ingredient

    Purified water (99.05%)

  • Purpose

    Eyewash

  • Uses

    washes the eye to help relieve

    • irritation
    • discomfort
    • burning
    • stinging
    • itching

    by removing

    • loose foreign material
    • air pollutants (smog or pollen)
    • chlorinated water
  • Warnings

    For external use only

    Do not use

    • if you have open wounds in or near the eyes, and get medical help right away
    • if solution changes color or becomes cloudy

    When using this product

    • remove contact lenses before using
    • do not touch to of container to any surface to avoid contamination
    • replace cap after use

    Stop use and ask a doctor if

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

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Directions

    For use with nozzle applicator.

    • flush the affected eye(s) as needed
    • control the rate of flow of solution by pressure on the bottle
    • do not touch dropper tip to eye
  • Other information

    • store at 15°-25°C (59°-77°F)
    • keep tightly closed
    • does not contain thimerosal
    • use before expiration date marked on the bottle
  • Inactive ingredients

    boric acid, sodium borate and sodium chloride.

    PRESERVATIVE ADDED: benzalkonium chloride (0.01%)

  • Questions or comments?

    Call: 1-888-527-4276

  • Medic's Choice Soothing Eye Wash 118mL

    Medic's Choice Soothing Eye Wash 118mL

  • INGREDIENTS AND APPEARANCE
    MEDICS CHOICE SOOTHING EYE WASH 
    purified water solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55651-555
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER99.05 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    BORIC ACID (UNII: R57ZHV85D4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55651-555-01118 mL in 1 BOTTLE; Type 0: Not a Combination Product11/30/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01811/30/2024
    Labeler - KC Pharmaceuticals, Inc. (174450460)
    Establishment
    NameAddressID/FEIBusiness Operations
    Bausch & Lomb Inc.114406598manufacture(55651-555)
    Establishment
    NameAddressID/FEIBusiness Operations
    KC Pharmaceuticals, Inc.174450460pack(55651-555) , label(55651-555)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!