GOODSENSE LUBRICANT EYE DROPS (POLYETHYLENE GLYCOL 400) SOLUTION [HANLIM PHARM. CO., LTD.]

GOODSENSE LUBRICANT EYE DROPS (POLYETHYLENE GLYCOL 400) SOLUTION [HANLIM PHARM. CO., LTD.]
PDF | XML

NDC 11716-0042-7
Set ID eb0f7264-29d6-405d-8102-b7f902f2482d
Category HUMAN OTC DRUG LABEL
Packager HANLIM PHARM. CO., LTD.
Generic Name
Product Class
Product Number
Application Number PART349
  • ACTIVE INGREDIENT

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

    Polyethylene Glycol 400 (0.4%) ---------------------------------------------------Lubricant

    Propylene Glycol (0.3%) --------------------------------------------------------------Lubricant

  • PURPOSE

    Uses

    For the temporary relief of burning and irritation due to eye dryness.

  • WARNINGS

    Warnings

    For external use only.

  • DO NOT USE

    Do not use

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

    When using this product

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

    Stop use and ask a doctor if

    • you experience eye pain
    • changes in vision occur
    • redness or irritation of the eye(s) gets worse or lasts 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, Chlorhexidine Gluconate, Hydrochloric Acid, Hydroxypropyl Guar, Magnesium Chloride, Potassium Chloride, Purified Water, Sodium Chloride, Zinc Chloride

  • PRINCIPAL DISPLAY PANEL

    image of carton labelEnter section text here

  • INGREDIENTS AND APPEARANCE
    GOODSENSE LUBRICANT EYE DROPS 
    polyethylene glycol 400 solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11716-0042
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL - UNII:3WJQ0SDW1A) POLYETHYLENE GLYCOL 4000.4 mL  in 1 mL
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL0.3 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BORIC ACID (UNII: R57ZHV85D4)  
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
    CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    ZINC CHLORIDE (UNII: 86Q357L16B)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11716-0042-71 in 1 CARTON
    115 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34908/04/2010
    Labeler - HANLIM PHARM. CO., LTD. (687986034)

Related Drugs