WALGREENS LUBRICANT EYE (SODIUM CARBOXYMETHYLCELLULOSE) SOLUTION/ DROPS [WALGREEN COMPANY]

WALGREENS LUBRICANT EYE (SODIUM CARBOXYMETHYLCELLULOSE) SOLUTION/ DROPS [WALGREEN COMPANY]
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NDC 0363-0084-15
Set ID 67dfba36-b8ea-7d93-e053-2a91aa0a429f
Category HUMAN OTC DRUG LABEL
Packager Walgreen Company
Generic Name
Product Class
Product Number
Application Number PART349
  • ACTIVE INGREDIENT

    Active ingredients Purpose

    Sodium carboxymethycellulose 0.25%..................................Lubricant

  • PURPOSE

    Uses

    • As a lubricant to relieve dryness of the eye
    • As a protectant against further irritation of the eye
    • For temporary relief of burning, irritation, and discomfort including exposure to wind or sun
  • WARNINGS

    Warnings

    For external use only

    • To avoid contamination do not touch tip of opened container to any surface. Replace cap after using.
  • DO NOT USE

    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
    • 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 right away.

  • INDICATIONS & USAGE

    Directions

    • Instill 1 or 2 drops in the affected eye(s) as needed.
  • STORAGE AND HANDLING

    Other information

    • Store at room temperature.
  • INACTIVE INGREDIENT

    Inactive ingredients

    benzalkonium chloride, boric acid, calcium chloride, magnesium chloride, potassium chloride, sodium bicarbonate, sodium borate, sodium chloride, sodium dihydrogen phosphate monohydrate, water

  • DOSAGE & ADMINISTRATION

    Distributed by:

    Walgreen Co.

    200 Wilmont Rd.

    Deerfield, IL 60015

    Made in South Korea

  • PRINCIPAL DISPLAY PANEL

    placeholder

  • INGREDIENTS AND APPEARANCE
    WALGREENS LUBRICANT EYE 
    sodium carboxymethylcellulose solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0084
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM2.5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  
    WATER (UNII: 059QF0KO0R)  
    BORIC ACID (UNII: R57ZHV85D4)  
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-0084-151 in 1 BOX06/04/2018
    115 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34906/04/2018
    Labeler - Walgreen Company (008965063)

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