LUMIGAN- bimatoprost solution/ drops

LUMIGAN by

Drug Labeling and Warnings

LUMIGAN by is a Prescription medication manufactured, distributed, or labeled by Allergan, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Principal Display Panel - 0.3 mg/1 mL Carton Label

®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

Principal Display Panel - 0.3 mg/1 mL Carton Label

®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

Principal Display Panel - 0.3 mg/1 mL Carton Label

®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

INGREDIENTS AND APPEARANCE

LUMIGAN 
bimatoprost solution/ drops

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 0023-9187
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BIMATOPROST (UNII: QXS94885MZ) (BIMATOPROST - UNII:QXS94885MZ)	BIMATOPROST	0.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0023-9187-01	1 in 1 CARTON	03/22/2001
1		2.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2	NDC: 0023-9187-03	1 in 1 CARTON	03/22/2001
2		2.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
3	NDC: 0023-9187-05	1 in 1 CARTON	03/22/2001
3		5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
4	NDC: 0023-9187-07	1 in 1 CARTON	03/22/2001
4		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
EXPORT ONLY		03/22/2001

Labeler - Allergan, Inc. (144796497)