Label: FOCUS TEARS PF- carboxymethylcellulose sodium solution/ drops

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

Drug Label Information

Updated July 17, 2025

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  • Active ingredient

    Carboxymethylcellulose sodium (0.5%)

  • Purpose

    Eye Lubricant

  • Warnings

    For use in the eyes only.

  • When using this product

    ■ do not touch tip of container to any surface to avoid contamination.
    ■ do not reuse; once opened discard.

  • Stop use and ask a doctor if

    ■ you experience eye pain, changes in vision, continued redness or irritation of the eye.
    ■ tile 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 right away.

  • Directions

    ■ Instill 1 or 2 drops into affected eye(s) as needed and discard container.

  • Other information

    ■ Use only if tamper seal on top and bottom flaps are intact.
    ■ Store between 15°-30°C (59°-86°F).
    ■ Keep carton for complete product information.

  • Inactive ingredients

    Calcium chloride, magnesium chloride, potassium chloride, purified water, sodium chloride, sodium lactate. May also contain hydrochloric acid and/or sodium hydroxide to adjust pH.

  • PRINCIPAL DISPLAY PANEL

    Principal Display Panel

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  • INGREDIENTS AND APPEARANCE
    FOCUS TEARS PF 
    carboxymethylcellulose sodium solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82724-009
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM LACTATE (UNII: TU7HW0W0QT)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82724-009-2030 in 1 BOX09/01/2025
    10.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01809/01/2025
    Labeler - Covalent Medical (112467517)
    Establishment
    NameAddressID/FEIBusiness Operations
    Unither Manufacturing LLC079176615manufacture(82724-009)
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