LUMIGAN- bimatoprost solution/ drops 
Allergan, Inc.

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Lumigan 03

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

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™

Rx

(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
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 0.03%
Ophthalmic solution

3 mL

sterile

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

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)

Revised: 12/2018
Document Id: a2b1c1ee-5c60-4485-8f60-f027d665139b
Set id: ec9097e7-4be4-4e62-99c3-24b48244c9f2
Version: 9
Effective Time: 20181207
 
Allergan, Inc.