LUMIFY Redness Reliever Eye Drops

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: LUMIFY Redness Reliever Eye Drops
Generic name: BRIMONIDINE TARTRATE
Manufacturer: Bausch & Lomb Incorporated
Product type: HUMAN OTC DRUG
SPL set ID: 022de945-0b26-40ae-8e88-d3fe2464d106
SPL ID: 4e5af967-1d35-5b67-e063-6294a90a9296
Version: 17
Effective date: 2026-03-31
Source export date: 2026-09-28
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:35:54

Harmonized routes table
Harmonized routes
OPHTHALMIC

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 29 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application applno	NDA	208144	derived:openfda.application_number
application number		NDA208144	openfda.application_number
brand name		LUMIFY Redness Reliever Eye Drops	openfda.brand_name
generic name		BRIMONIDINE TARTRATE	openfda.generic_name
manufacturer name		Bausch & Lomb Incorporated	openfda.manufacturer_name
ndc	package	24208-537-25	openfda.package_ndc
ndc	package	24208-537-05	openfda.package_ndc
ndc	package	24208-537-99	openfda.package_ndc
ndc	package	24208-537-15	openfda.package_ndc
ndc	package	24208-537-01	openfda.package_ndc
ndc	package	24208-537-10	openfda.package_ndc
ndc	package	24208-537-35	openfda.package_ndc
ndc	package	24208-537-08	openfda.package_ndc
ndc	package	24208-537-75	openfda.package_ndc
ndc	product	24208-537	openfda.product_ndc
ndc11	package	24208053775	derived:openfda.package_ndc
ndc11	package	24208053710	derived:openfda.package_ndc
ndc11	package	24208053701	derived:openfda.package_ndc
ndc11	package	24208053735	derived:openfda.package_ndc
ndc11	package	24208053708	derived:openfda.package_ndc
ndc11	package	24208053705	derived:openfda.package_ndc
ndc11	package	24208053725	derived:openfda.package_ndc
ndc11	package	24208053799	derived:openfda.package_ndc
ndc11	package	24208053715	derived:openfda.package_ndc
rxcui		1999016	openfda.rxcui
rxcui		1999021	openfda.rxcui
spl id		4e5af967-1d35-5b67-e063-6294a90a9296	id
spl set id		022de945-0b26-40ae-8e88-d3fe2464d106	set_id
unii		4S9CL2DY2H	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

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.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.