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

  • NDC Code(s): 24208-537-01, 24208-537-05, 24208-537-08, 24208-537-10, view more
    24208-537-15, 24208-537-25, 24208-537-35, 24208-537-75, 24208-537-99
  • Packager: Bausch & Lomb Incorporated
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Drug Application

Drug Label Information

Updated November 6, 2023

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  • Active ingredient

    Brimonidine tartrate (0.025%)

  • Purpose

    Redness reliever

  • Use

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

  • 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
  • Other information

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

  • Questions or comments?

    Call: 1-800-553-5340

  • PRINCIPAL DISPLAY PANEL - 7.5 mL Carton

    cartonBAUSCH + LOMB

    NDC 24208-537-25

    LARGE
    SIZE

    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)

    AB53708

    3838702

  • INGREDIENTS AND APPEARANCE
    LUMIFY REDNESS RELIEVER EYE DROPS 
    brimonidine tartrate solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24208-537
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BRIMONIDINE TARTRATE (UNII: 4S9CL2DY2H) (BRIMONIDINE - UNII:E6GNX3HHTE) BRIMONIDINE TARTRATE0.25 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    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 CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:24208-537-251 in 1 CARTON12/22/2017
    17.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    2NDC:24208-537-081 in 1 CARTON12/22/2017
    22.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    3NDC:24208-537-991 in 1 CARTON12/22/2017
    32.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    4NDC:24208-537-751 in 1 CARTON12/22/2017
    47.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    5NDC:24208-537-101 in 1 CARTON05/01/2019
    50.4 mL in 1 AMPULE; Type 0: Not a Combination Product
    6NDC:24208-537-011 in 1 CARTON05/01/2019
    60.4 mL in 1 AMPULE; Type 0: Not a Combination Product
    7NDC:24208-537-152 in 1 CARTON04/30/2019
    77.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    8NDC:24208-537-051 in 1 CARTON09/25/2020
    85 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    9NDC:24208-537-351 in 1 CARTON05/02/2023
    93.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA20814412/22/2017
    Labeler - Bausch & Lomb Incorporated (196603781)
    Establishment
    NameAddressID/FEIBusiness Operations
    Bausch & Lomb Incorporated079587625MANUFACTURE(24208-537)
    Establishment
    NameAddressID/FEIBusiness Operations
    Laboratoire Unither574139809MANUFACTURE(24208-537)
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