Label: MEDICS CHOICE EYE DROPS SEASONAL RELIEF- tetrahydrozoline hydrochloride, zinc sulfate solution/ drops

  • NDC Code(s): 55651-024-01
  • Packager: KC Pharmaceuticals, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 4, 2024

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  • ACTIVE INGREDIENT

    Active ingredients

    Tetrahydrozoline HCl 0.05%

    Zinc sulfate 0.25%

  • PURPOSE

    Purposes

    Tetrahydrozoline HCl.....Redness reliever

    Zinc sulfate...............Astringent

  • INDICATIONS & USAGE

    Use

    ■ for temporary relief of discomfort and redness of the eye due to minor eye irritations

  • WARNINGS

    Warnings

    For external use only

    Ask a doctor before use 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 breast-feeding, ask a health professional before use.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center

    (1-800-222-1222) right away.

  • DOSAGE & ADMINISTRATION

    Directions

    instill 1 to 2 drops in the affected eye(s) up to 4 times daily

  • OTHER SAFETY INFORMATION

    Other information

    store at 15°-30°C (59°-86°F)

  • INACTIVE INGREDIENT

    Inactive ingredients

    benzalkonium chloride, boric acid, edetate disodium, purified water, sodium chloride, sodium citrate

  • PRINCIPAL DISPLAY PANEL

    Carton

  • INGREDIENTS AND APPEARANCE
    MEDICS CHOICE EYE DROPS SEASONAL RELIEF 
    tetrahydrozoline hydrochloride, zinc sulfate solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55651-024
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC SULFATE (UNII: 89DS0H96TB) (ZINC CATION - UNII:13S1S8SF37) ZINC SULFATE2.5 mg  in 1 mL
    TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D) (TETRAHYDROZOLINE - UNII:S9U025Y077) TETRAHYDROZOLINE HYDROCHLORIDE0.5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    BORIC ACID (UNII: R57ZHV85D4)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55651-024-011 in 1 CARTON10/23/2003
    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 DrugM01810/23/2003
    Labeler - KC Pharmaceuticals, Inc. (174450460)
    Establishment
    NameAddressID/FEIBusiness Operations
    KC Pharmaceuticals, Inc.174450460manufacture(55651-024) , pack(55651-024) , label(55651-024)
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