Label: VENTIVA TEARS LUBRICANT EYE DROPS- carboxymethylcellulose sodium liquid

  • NDC Code(s): 83035-8030-5
  • Packager: Singular Dreamer Ltd.dba True Marker
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 1, 2024

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  • Active Ingredient

    CARBOXYMETHYLCELLULOSE SODIUM 0.5%

  • Purpose

    Lubricant

  • Uses

    For the temporary relief of burning and irritation due to dryness of the eye, for the temporary relief of discomfort due to minor
    irritations of the eye or to exposure to wind or sun. May be used as a protectant against further irritation.

  • Warnings

    For external use only

    Do not use

    • if this product changes color or becomes cloudy
    • if you are sensitive to any ingredient in this product

    When using this product

    • do not touch tip of container to any surface to avoid contamination
    • replace cap after each use

    Stop use and ask a doctorif you experience any of the
    following:

    • eye pain 
    • change in vision
    • continued redness or irritation of the eye
    • 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.(1-800-222-1222) right away.

  • KEEP OUT OF REACH OF CHILDREN

  • Directions

    Shake well before using. Put 1 or 2 drops in the affected eye (s) as needed.

  • Other Information

    store at room temperature.

  • Inactive Ingredients

    water, boric acid, potassium chloride, calcium chloride, magnesium chloride, sodium chlorate, chlorine dioxide, sodium borate, sodium chloride, hydrochloric acid, sodium hydroxide

  • Questions ?

    1-888-811-2634

  • Product label

    image description
    image description
  • INGREDIENTS AND APPEARANCE
    VENTIVA TEARS LUBRICANT EYE DROPS 
    carboxymethylcellulose sodium liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83035-8030
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED0.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    BORIC ACID (UNII: R57ZHV85D4)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    SODIUM CHLORATE (UNII: T95DR77GMR)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83035-8030-51 in 1 CARTON01/01/2024
    115 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01801/01/2024
    Labeler - Singular Dreamer Ltd.dba True Marker (129504103)
    Registrant - Singular Dreamer Ltd.dba True Marker (129504103)
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