Label: WALGREENS LUBRICANT EYE- carboxymethylcellulose sodium solution

  • 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 September 30, 2012

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  • ACTIVE INGREDIENT

    Active ingredient                                                                     Purpose

    Carboxymethylcellulose Sodium 0.5%......................................Lubricant

  • PURPOSE

    Uses

    • For the temporary relief of burning 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

  • DO NOT USE

    To avoid contamination, do not touch tip of container to any surface

    Replace cap after using.  Do not use if solution changes color or becomes cloudy.

  • STOP USE

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

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of children.

    • If swallowed, get medical help or contact a Poison Control Center immediately
    • Retain carton for future reference.
  • INDICATIONS & USAGE

    Directions

    • Put 1 or 2 drops in the affected eye/s as needed
  • STORAGE AND HANDLING

    Other information

    • store at room temperature 15o to 30oC (59o to 86oF)
  • INACTIVE INGREDIENT

    Boric Acid, Calcium Chloride, Magnesium Chloride, Potassium Chloride, Sterile Purified Water, Benzalkonium Chloride, Sodium Borate, Sodium Chloride

  • DOSAGE & ADMINISTRATION

    DISTRIBUTED BY: WALGREEN CO.

    200 WILMOT RD., DEERFIELD, IL 60015

    walgreens.com

    Made in Korea

  • PRINCIPAL DISPLAY PANEL

    image of carton label

  • INGREDIENTS AND APPEARANCE
    WALGREENS LUBRICANT EYE  
    carboxymethylcellulose sodium solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-1466
    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
    BORIC ACID (UNII: R57ZHV85D4)  
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-1466-302 in 1 CARTON
    115 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34909/30/2012
    Labeler - WALGREEN COMPANY (008965063)
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