Label: LUMIFY REDNESS RELIEVER EYE DROPS- brimonidine tartrate solution/ drops

  • NDC Code(s): 24208-537-01, 24208-537-08, 24208-537-10, 24208-537-15, view more
    24208-537-25, 24208-537-75, 24208-537-99
  • Packager: Bausch & Lomb Incorporated
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated May 27, 2019

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • Active ingredient

    Brimonidine tartrate (0.025%)

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  • Purpose

    Redness reliever

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  • Use

    relieves redness of the eye due to minor eye irritations
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  • Warnings

    For external use only

    Do not use

    if solution changes color or becomes cloudy

    Stop use and ask a doctor if

    you experience eye pain, changes in vision, continued redness or irritation of the eye
    condition worsens or persists for more than 3 days

    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 right away.

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  • Directions

    adults and children 5 years of age and over:
    instill 1 drop in the affected eye(s) every 6-8 hours
    do not use more than 4 times daily
    remove contact lenses before use
    wait at least 10 minutes before re-inserting contact lenses after use
    if using other ophthalmic products while using this product, wait at least 5 minutes between each product
    to avoid contamination, do not touch tip of container to any surface
    replace cap after each use
    children under 5 years of age: consult a doctor
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  • Other information

    store at 15°-25°C (59°-77°F)
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  • Inactive ingredients

    benzalkonium chloride, boric acid, calcium chloride dihydrate, glycerin, potassium chloride, sodium borate decahydrate, sodium chloride. water for injection. Hydrochloric acid and/or sodium hydroxide may be used to adjust pH.

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  • Questions or comments?

    Call: 1-800-553-5340

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  • PRINCIPAL DISPLAY PANEL - 7.5 mL Carton

    BAUSCH + LOMB

    NDC 24208-537-25

    [eye image]

    LUMIFY

    BRIMONIDINE TARTRATE

    OPHTHALMIC SOLUTION 0.025%

    REDNESS RELIEVER EYE DROPS

    Works in 1 minute
    Lasts up to 8 hours

    Sterile 0.25 FL OZ (7.5 mL)

    carton.jpg
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  • INGREDIENTS AND APPEARANCE
    LUMIFY REDNESS RELIEVER EYE DROPS 
    brimonidine tartrate solution/ drops
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:24208-537
    Route of Administration OPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BRIMONIDINE TARTRATE (UNII: 4S9CL2DY2H) (BRIMONIDINE - UNII:E6GNX3HHTE) BRIMONIDINE TARTRATE 0.25 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    BORIC ACID (UNII: R57ZHV85D4)  
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:24208-537-25 1 in 1 CARTON 12/22/2017
    1 7.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    2 NDC:24208-537-08 1 in 1 CARTON 12/22/2017
    2 2.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    3 NDC:24208-537-99 1 in 1 CARTON 12/22/2017
    3 2.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    4 NDC:24208-537-75 1 in 1 CARTON 12/22/2017
    4 7.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    5 NDC:24208-537-10 1 in 1 CARTON 05/01/2019
    5 0.4 mL in 1 AMPULE; Type 0: Not a Combination Product
    6 NDC:24208-537-01 1 in 1 CARTON 05/01/2019
    6 0.4 mL in 1 AMPULE; Type 0: Not a Combination Product
    7 NDC:24208-537-15 2 in 1 CARTON 04/30/2019
    7 7.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    NDA NDA208144 12/22/2017
    Labeler - Bausch & Lomb Incorporated (196603781)
    Establishment
    Name Address ID/FEI Business Operations
    Bausch & Lomb Incorporated 079587625 MANUFACTURE(24208-537)
    Establishment
    Name Address ID/FEI Business Operations
    Laboratoire Unither 574139809 MANUFACTURE(24208-537)
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