LUMIFY REDNESS RELIEVER EYE DROPS- brimonidine tartrate solution/ drops 
Bausch & Lomb Incorporated

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Drug Facts

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

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
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)

Revised: 5/2019
Document Id: 048b65cd-c120-48ea-a115-f59048e4198c
Set id: 022de945-0b26-40ae-8e88-d3fe2464d106
Version: 5
Effective Time: 20190527
 
Bausch & Lomb Incorporated