Label: GOOD NEIGHBOR PHARMACY EYE DROPS ADVANCED RELIEF- dextran 70, polyethylene glycol 400, povidone, tetrahydrozoline hydrochloride solution/ drops

  • NDC Code(s): 24385-077-05
  • Packager: AmerisourceBergen Drug Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 20, 2023

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  • Drug Facts

  • Active Ingredients

    Dextran 70 0.1%

    Polyethylene glycol 400 1%

    Povidone 1%

    Tetrahydrozoline HCl 0.05%

  • Purpose

    Eye lubricant and Redness reliever

  • Uses

    relieves redness of the eye due to minor eye irritations

    as a lubricant to prevent further irritation or to relieve dryness of the eye

  • Warnings

    For external use only

    Ask a doctor before us if

    you have narrow angle glaucoma

    when using this product

    pupils may become enlarged temporarily

    to avoid contamination, do not touch tip of container to any surface. Replace cap after using.

    if solution changes color or becomes cloudy,do not use

    overuse may produce increased redness of the eye

    remove contact lens before using

    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

    If pregnant or breastfeeding

    ask a health professional before use.

  • Keep out of reach of children

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

  • Directions

    Instill 1 or 2 drops in the affected eye(s) up to four times daily

  • Other information

    Store at 15 °-30°C (59°-86°F)

  • Inactive ingredients

    benzalkonium chloride,

    boric acid, edetate

    disodium, purified

    water, sodium borate,

    and sodium chloride

  • Good Neighbor Pharmacy Eye Drops

    24385007705.jpg

  • INGREDIENTS AND APPEARANCE
    GOOD NEIGHBOR PHARMACY EYE DROPS  ADVANCED RELIEF
    dextran 70, polyethylene glycol 400, povidone, tetrahydrozoline hydrochloride solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24385-077
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTRAN 70 (UNII: 7SA290YK68) (DEXTRAN 70 - UNII:7SA290YK68) DEXTRAN 700.1 g  in 100 mL
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ) POLYETHYLENE GLYCOL 4001 g  in 100 mL
    POVIDONE (UNII: FZ989GH94E) (POVIDONE - UNII:FZ989GH94E) POVIDONE1 g  in 100 mL
    TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D) (TETRAHYDROZOLINE - UNII:S9U025Y077) TETRAHYDROZOLINE HYDROCHLORIDE0.05 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    BORIC ACID (UNII: R57ZHV85D4)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:24385-077-051 in 1 CARTON01/29/2001
    115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01801/29/2001
    Labeler - AmerisourceBergen Drug Corporation (007914906)
    Registrant - K.C. Pharmaceuticals, Inc. (174450460)
    Establishment
    NameAddressID/FEIBusiness Operations
    KC Pharmaceuticals, Inc174450460manufacture(24385-077) , label(24385-077) , pack(24385-077)
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