Label: RESTORE PLUS SINGLE VIAL- carboxmethylcellulose sodium solution/ drops

  • Category: HUMAN OTC DRUG LABEL

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.

Drug Label Information

Updated November 10, 2021

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  • ACTIVE INGREDIENT

    Active ingredient Purpose

    Carboxymethylcellulose sodium 0.5%.........................Eye lubricant

  • PURPOSE

    Uses

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

    Warnings

    For external use only.

    • to avoid contamination, do not touch tip of container to any surface. Do not reuse. Once opened, discard.
    • do not touch unit-dose tip to eyes.
    • if solution changes color or becomes cloudy, do not use
  • STOP USE

    Stop use and ask a doctor if you experience eye pain changes in vision, continued redness or irritation of the eye, or in the condtion worsens or persists for more than 72 hours

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • INDICATIONS & USAGE

    Directions

    To open, twist and pull tab to remove. Instill 1 or 2 drops in the affected eye(s) as needed and discard container.

    if used for post-operative (e.g. LASIK) dryness and discomfort, follow your eye doctor's instructions

  • STORAGE AND HANDLING

    Other information

    • use only if single-use container is intact
    • use before expiration date marked on container
    • store at 59°-86°F (15°-30°C)
    • retain carton for future reference
  • INACTIVE INGREDIENT

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

  • DOSAGE & ADMINISTRATION

    Distributed by:

    Wal-Mart Stores, Inc.

    Bentonville, AR 72716

    Made in Korea

  • PRINCIPAL DISPLAY PANEL

    single

  • INGREDIENTS AND APPEARANCE
    RESTORE PLUS SINGLE VIAL 
    carboxmethylcellulose sodium solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65923-657
    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
    SODIUM LACTATE (UNII: TU7HW0W0QT)  
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65923-657-040.4 mL in 1 VIAL; Type 0: Not a Combination Product01/01/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34901/01/2016
    Labeler - United Exchange Corp. (840130579)
    Registrant - United Exchange Corp. (840130579)