Label: LUMIGAN- bimatoprost solution/ drops

  • NDC Code(s): 0023-9187-01, 0023-9187-03, 0023-9187-05, 0023-9187-07
  • Packager: Allergan, Inc.
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Export only

Drug Label Information

Updated December 10, 2018

If you are a consumer or patient please visit this version.

  • Principal Display Panel - 0.3 mg/1 mL Carton Label

    ®ALLERGAN

    LUMIGAN®
    (bimatoprost
    ophthalmic solution)

    0.03%

    3 mL

    sterile Rx only

    ®ALLERGAN
LUMIGAN®
(bimatoprost
ophthalmic solution) 
0.03% 
3 mL
sterile Rx only

  • Principal Display Panel - 0.3 mg/1 mL Carton Label

    ALLERGAN™

    Rx

    BIMATOPROST
    OPHTHALMIC
    SOLUTION 0.03%

    LUMIGAN™

    3 mL

    sterile

    FOR EXTERNAL USE ONLY

    ALLERGAN™
Rx 
BIMATOPROST
OPHTHALMIC
SOLUTION 0.03% 
LUMIGAN™
3 mL
sterile 
FOR EXTERNAL USE ONLY

  • Principal Display Panel - 0.3 mg/1 mL Carton Label

    ®ALLERGAN

    LUMIGAN™

    (BIMATOPROST
    OPHTHALMIC
    SOLUTION)
    0.03%

    3 mL

    sterile

    ®ALLERGAN
LUMIGAN™
(BIMATOPROST
OPHTHALMIC
SOLUTION)
0.03% 
3 mL
sterile

  • Principal Display Panel - 0.3 mg/1 mL Carton Label

    ®ALLERGAN

    LUMIGAN™

    (BIMATOPROST
    OPHTHALMIC
    SOLUTION)
    0.03%

    K

    3 mL

    sterile

    ®ALLERGAN
LUMIGAN™
(BIMATOPROST
OPHTHALMIC
SOLUTION)
0.03% 
K
3 mL
sterile

  • Principal Display Panel - 0.3 mg/1 mL Carton Label

    ®ALLERGAN

    LUMIGAN™

    (BIMATOPROST
    OPHTHALMIC
    SOLUTION)
    0.03%

    3 mL

    sterile

    ®ALLERGAN
LUMIGAN™
(BIMATOPROST
OPHTHALMIC
SOLUTION)
0.03% 
3 mL
sterile

  • Principal Display Panel - 0.3 mg/1 mL Carton Label

    ®ALLERGAN

    LUMIGAN™

    (BIMATOPROST
    OPHTHALMIC
    SOLUTION)
    0.03%

    3 mL

    sterile

    ®ALLERGAN
LUMIGAN™
(BIMATOPROST
OPHTHALMIC
SOLUTION)
0.03% 
3 mL
sterile

  • INGREDIENTS AND APPEARANCE
    LUMIGAN 
    bimatoprost solution/ drops
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:0023-9187
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BIMATOPROST (UNII: QXS94885MZ) (BIMATOPROST - UNII:QXS94885MZ) BIMATOPROST0.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0023-9187-011 in 1 CARTON03/22/2001
    12.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    2NDC:0023-9187-031 in 1 CARTON03/22/2001
    22.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    3NDC:0023-9187-051 in 1 CARTON03/22/2001
    35 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    4NDC:0023-9187-071 in 1 CARTON03/22/2001
    47.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    EXPORT ONLY03/22/2001
    Labeler - Allergan, Inc. (144796497)