GOODSENSE LUBRICATING EYE DROPS (CARBOXYMETHYLCELLULOSE SODIUM) SOLUTION [HANLIM PHARM. CO., LTD.]

GOODSENSE LUBRICATING EYE DROPS (CARBOXYMETHYLCELLULOSE SODIUM) SOLUTION [HANLIM PHARM. CO., LTD.]
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NDC 11716-0041-8
Set ID f8493cb0-ae0a-485c-86b5-da26e7f49453
Category HUMAN OTC DRUG LABEL
Packager HANLIM PHARM. CO., LTD.
Generic Name
Product Class
Product Number
Application Number PART349
  • ACTIVE INGREDIENT

    Active ingredients----------------------------------------------------------Purpose

    Carboxymethylcellulose Sodium 0.5%----------------------------Lubricant

    Glycerin 0.9%---------------------------------------------------------------Lubricant

  • PURPOSE

    Uses

    • For the temporary relief of burning, irritation, and discomfort due to dryness of the eye or from irritation from wind or sun.
    • May be sued to protect against further irritation.
  • WARNINGS

    Warnings

    • For external use only.
  • WHEN USING

    When using this product

    • To avoid contamination, do not touch tip of container to any surface.  Replace cap after using.
    • Do not use if solution changes color or gets cloudy.
  • STOP USE

    Stop use and ask a doctor if

    You feel 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 reach of children.

    If swallowed, get medical help or contact a Poison Control Center immediately.

  • INDICATIONS & USAGE

    Directions

    Put 1 or 2 drops in the affected eye/s as needed.

  • INACTIVE INGREDIENT

    Inactive ingredients: Boric Acid, Calcium Chloride Dihydrate, Chlorhexidine Gluconate, Erythritol Hexahydrate, Levocarnitine, Magnesium Chloride, Potassium Chloride, Purified Water, Sodium Borate Decahydrate, Sodium Citrate Dihydrate

  • PRINCIPAL DISPLAY PANEL

    image of carton labelEnter section text here

  • INGREDIENTS AND APPEARANCE
    GOODSENSE LUBRICATING EYE DROPS 
    carboxymethylcellulose sodium solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11716-0041
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM5 mg  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN9 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BORIC ACID (UNII: R57ZHV85D4)  
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
    CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)  
    ERYTHRITOL (UNII: RA96B954X6)  
    LEVOCARNITINE (UNII: 0G389FZZ9M)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11716-0041-81 in 1 CARTON
    115 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34907/30/2010
    Labeler - HANLIM PHARM. CO., LTD. (687986034)

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