Label: EQUATE OPTIMAL HYDRATION LUBRICANT EYE DROPS- carboxymethylcellulose sodium, glycerin solution/ drops

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 1, 2024

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

View All Sections
  • Active ingredients

    Carboxymethylcellulose sodium 0.5%

    Glycerin 0.9%

  • Purposes

    Lubricant

    Lubricant

  • Uses

    • for use as a protectant against further irritation or to relieve dryness of the eye
    • for temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun
  • Warnings

    For external use only

    Do not use this product if

    • solution changes color or becomes cloudy

    When using this product

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

    Stop use and ask a doctor if you experience

    • eye pain
    • changes in vision
    • continued redness or irritation
    • condition worsens or persists for more than 72 hours

    Keep out of reach of children.

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

  • Directions

    instill 1 to 2 drops in the affected eye(s) as needed

  • Other information

    • store at 15-25°C (59-77°F)
      • RETAIN THIS CARTON FOR FUTURE REFERENCE
  • Inactive ingredients

    benzalkonium chloride, boric acid, calcium chloride hydrate (dihydrate), magnesium chloride, potassium chloride, sodium borate, sodium citrate hydrate, water for injection

  • Questions or comments?

    Call 1-888-287-1915

  • Equate Optimal Hydration Lubricant Eye Drops 15mL

    Equate Optimal Hydration Lubricant Eye Drops 15mL

  • INGREDIENTS AND APPEARANCE
    EQUATE OPTIMAL HYDRATION LUBRICANT EYE DROPS 
    carboxymethylcellulose sodium, glycerin solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-258
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM0.5 g  in 100 mL
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN0.9 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    WATER (UNII: 059QF0KO0R)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    BORIC ACID (UNII: R57ZHV85D4)  
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79903-258-051 in 1 BOX04/01/2024
    115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01804/01/2024
    Labeler - Walmart, Inc. (051957769)
    Registrant - KC Pharmaceuticals, Inc. (174450460)
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!