DailyMed - 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 January 29, 2025

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

Download DRUG LABEL INFO: PDF XML
Official Label (Printer Friendly)

View All Sections

Active ingredient
Brimonidine tartrate (0.025%)

Brimonidine tartrate (0.025%)
Close
Purpose
Redness reliever

Redness reliever
Close
Use
relieves redness of the eye due to minor eye irritations
- relieves redness of the eye due to minor eye irritations
Close
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 ...
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.

Close
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 ...
- 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
Close
Other information
store at 15-25°C (59-77°F)
- store at 15-25°C (59-77°F)
Close
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 ...

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.
Close
Questions or comments?
[phone icon] Call: 1-800-553-5340

[phone icon] Call: 1-800-553-5340
Close
PRINCIPAL DISPLAY PANEL - 7.5 mL Carton
BAUSCH + LOMB - 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 ...
BAUSCH + LOMB

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

3911700
Close

INGREDIENTS AND APPEARANCE

Product Information

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

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BRIMONIDINE TARTRATE (UNII: 4S9CL2DY2H) (BRIMONIDINE - UNII:E6GNX3HHTE)	BRIMONIDINE TARTRATE	0.25 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date
Packaging
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
8	NDC:24208-537-05	1 in 1 CARTON	09/25/2020
8		5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
9	NDC:24208-537-35	1 in 1 CARTON	05/02/2023
9		3.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
NDA	NDA208144	12/22/2017

Labeler - Bausch & Lomb Incorporated (196603781)

Name	Address	ID/FEI	Business Operations
Establishment
Bausch & Lomb Incorporated		079587625	manufacture(24208-537)

Name	Address	ID/FEI	Business Operations
Establishment
Laboratoire Unither		574139809	manufacture(24208-537)

Published Date (What is this?)	Version	Files
Jan 30, 2025	15 (current)	download
Nov 10, 2023	14	download
Nov 8, 2023	13	download
Jun 21, 2023	12	download
Nov 21, 2022	11	download
Apr 28, 2022	10	download
Jul 7, 2021	9	download
Dec 18, 2020	8	download
Oct 29, 2020	7	download
Jan 21, 2020	6	download
Aug 16, 2019	5	download
Aug 6, 2019	4	download
May 29, 2019	3	download
May 24, 2019	2	download
Feb 8, 2018	1	download

	RxCUI	RxNorm NAME	RxTTY
1	1999016	brimonidine tartrate 0.025 % Ophthalmic Solution	PSN
2	1999016	brimonidine tartrate 0.25 MG/ML Ophthalmic Solution	SCD
3	1999016	brimonidine tartrate 0.025 % Ophthalmic Solution	SY
4	1999021	LUMIFY 0.025 % Ophthalmic Solution	PSN
5	1999021	brimonidine tartrate 0.25 MG/ML Ophthalmic Solution [Lumify]	SBD
6	1999021	Lumify 0.025 % Ophthalmic Solution	SY
7	1999021	Lumify 0.25 MG/ML Ophthalmic Solution	SY

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

View Package Photos

Drug Label Info

Safety

Related Resources

More Info For This Drug

Drug Label Information

Do not use

Stop use and ask a doctor if

If pregnant or breast-feeding, ask a health professional before use.

Find additional resources

Safety

Related Resources

More Info on this Drug

	NDC
1	24208-537-01
2	24208-537-05
3	24208-537-08
4	24208-537-10
5	24208-537-15
6	24208-537-25
7	24208-537-35
8	24208-537-75
9	24208-537-99

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

View Package Photos

Drug Label Info

Safety

Related Resources

More Info For This Drug

Drug Label Information

Do not use

Stop use and ask a doctor if

If pregnant or breast-feeding, ask a health professional before use.

Find additional resources

Safety

Related Resources

More Info on this Drug

LUMIFY REDNESS RELIEVER EYE DROPS- brimonidine tartrate solution/ drops

Number of versions: 15

LUMIFY REDNESS RELIEVER EYE DROPS- brimonidine tartrate solution/ drops

LUMIFY REDNESS RELIEVER EYE DROPS- brimonidine tartrate solution/ drops

To receive this label RSS feed

To receive all DailyMed Updates for the last seven days

What will I get with the DailyMed RSS feed?

How to discontinue the RSS feed

Why is DailyMed no longer displaying pill images on the Search Results and Drug Info pages?

LUMIFY REDNESS RELIEVER EYE DROPS- brimonidine tartrate solution/ drops

If this SPL contains inactivated NDCs listed by the FDA initiated compliance action, they will be specified as such.