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Medication guide

Brimonidine: uses, appearance and warnings

What the official FDA label says Brimonidine is used for, what it looks like, and its most important warnings — in plain English, with the label text one click away.
alpha-Adrenergic AgonistPrescription label

Uses

What the official label says Brimonidine is used for

The FDA label for Brimonidine states:

Brimonidine tartrate ophthalmic solution 0.1% is indicated for the reduction of elevated intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension. Brimonidine tartrate ophthalmic solution is an alpha adrenergic receptor agonist indicated for the reduction of elevated intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension. ( 1 )
Read the label's “Indications and usage” section (verbatim)
Brimonidine tartrate ophthalmic solution 0.1% is indicated for the reduction of elevated intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension. Brimonidine tartrate ophthalmic solution is an alpha adrenergic receptor agonist indicated for the reduction of elevated intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension. ( 1 )

Names & forms

Brand names, forms and strengths

Brand names (from RxNorm; not every brand is still sold): Alphagan, Lumify.

Generic name: brimonidine · RxNorm ID (RxCUI): 134615

Forms and strengths of Brimonidine listed in RxNorm
FormStrengths listed in RxNorm
Ophthalmic Solution0.25 MG/ML, 1 MG/ML, 1.5 MG/ML, 2 MG/ML

Strengths are listed so you can recognise a product — not as dosing information. Only your prescriber can decide what is right for you.

Read the label's “Dosage forms and strengths” section (verbatim)
Ophthalmic solution containing 0.1% (1 mg/mL) brimonidine tartrate. Ophthalmic solution containing 0.1% (1 mg/mL) brimonidine tartrate. ( 3 )

Appearance

What Brimonidine looks like

The DailyMed product data we retrieved does not include colour or shape details for Brimonidine (common for ophthalmic products). Appearance varies by manufacturer — your pharmacist can confirm what yours should look like.

Read the label's “How supplied” section (verbatim)
Brimonidine tartrate ophthalmic solution is supplied sterile, in white opaque LDPE ophthalmic bottles with white translucent LDPE ophthalmic dropper and purple opaque ophthalmic HDPE plastic cap as follows: 0.1% 5 mL in 5 mL bottle NDC 60505-0577-1 10 mL in 11 mL bottle NDC 60505-0577-2 15 mL in 15 mL bottle NDC 60505-0577-3 Storage: Store at 20°C to 25°C (68°F to 77°F) [See USP Controlled Room temperature]. KEEP THIS AND ALL DRUGS OUT OF REACH OF CHILDREN

Safety

Important warnings for Brimonidine

Potentiation of vascular insufficiency. ( 5.1 ) 5.1 Potentiation of Vascular Insufficiency Brimonidine tartrate ophthalmic solution may potentiate syndromes associated with vascular insufficiency. Brimonidine tartrate ophthalmic solution should be used with caution in patients with depression, cerebral or coronary insufficiency, Raynaud's phenomenon, orthostatic hypotension, or thromboangiitis obliterans. …

Contraindications — who should not use it (verbatim)
Neonates and infants (pediatric patients younger than 2 years old). ( 4.1 ) Hypersensitivity Reactions. ( 4.2 ) 4.1 Neonates and Infants (Pediatric Patients Younger than 2 Years Old) Brimonidine tartrate ophthalmic solution is contraindicated in neonates and infants (pediatric patients younger than 2 years old) [see Use in Specific Populations ( 8.4 )]. 4.2 Hypersensitivity Reactions Brimonidine tartrate ophthalmic solution is contraindicated in patients who have exhibited a hypersensitivity reaction to any component of this medication in the past.
Warnings and precautions (verbatim excerpt)
Potentiation of vascular insufficiency. ( 5.1 ) 5.1 Potentiation of Vascular Insufficiency Brimonidine tartrate ophthalmic solution may potentiate syndromes associated with vascular insufficiency. Brimonidine tartrate ophthalmic solution should be used with caution in patients with depression, cerebral or coronary insufficiency, Raynaud's phenomenon, orthostatic hypotension, or thromboangiitis obliterans. 5.2 Severe Cardiovascular Disease Although brimonidine tartrate ophthalmic solution had minimal effect on the blood pressure of patients in clinical studies, caution should be exercised in treating patients with severe cardiovascular disease. 5.3 Contamination of Topical Ophthalmic Products After Use There have been reports of bacterial keratitis associated with the use of multiple-dose containers of topical ophthalmic products. These containers had been inadvertently contaminated by patients who, in most cases, had a concurrent corneal disease or a disruption of the ocular epithelial surface. Do not touch the tip of the dispensing container to the eye or surrounding structures. Serious damage to the eye and subsequent loss of vision may result from using contaminated solutions [see Patient Counseling Information ( 17 )].
Side effects — opening of the label's adverse reactions section
The following serious adverse reactions are described elsewhere in the labeling: Potentiation of Vascular Insufficiency [see Warnings and Precautions ( 5.1 )] Severe Cardiovascular Disease [see Warnings and Precautions ( 5.2 )] Contamination of Topical Ophthalmic Products after Use [see Warnings and Precautions ( 5.3 )] Neonates and Infants (Pediatric Patients Younger than 2 Years Old) [see Contraindications ( 4.1 )] Most common adverse reactions occurring in approximately 5% to 20% of patients receiving brimonidine ophthalmic solution (0.1% to 0.2%) included allergic conjunctivitis, burning sensation, conjunctival folliculosis, conjunctival hyperemia, eye pruritus, hypertension, ocular allergic reaction, oral dryness, and visual disturbance. ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Apotex Corp. at 1-800-706-5575 or the FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. …
Drug interactions — opening of the label's section
Antihypertensives/cardiac glycosides may lower blood pressure. ( 7.1 ) Use with CNS depressants may result in an additive or potentiating effect. ( 7.2 ) Tricyclic antidepressants may potentially blunt the hypotensive effect of systemic clonidine. ( 7.3 ) Monoamine oxidase inhibitors may result in increased hypotension. ( 7.4 ) 7.1 Antihypertensives/Cardiac Glycosides Because brimonidine tartrate ophthalmic solution may reduce blood pressure, caution in using drugs such as antihypertensives and/or cardiac glycosides with brimonidine tartrate ophthalmic solution is advised. 7.2 CNS Depressants Although specific drug interaction studies have not been conducted with brimonidine tartrate ophthalmic solution, the possibility of an additive or potentiating effect with CNS depressants (alcohol, barbiturates, opiates, sedatives, or anesthetics) should be considered. …

This is not a complete list of warnings or side effects. Read the full label and talk to your prescriber or pharmacist. To report a side effect to the FDA, use MedWatch.

Resources

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Sources

Label text is quoted from the Apotex Corp. label (label version effective September 9, 2026), retrieved October 20, 2026. Other manufacturers' labels for the same medicine may differ in wording.

If anything here differs from the label that came with your medicine, follow your label and your pharmacist.

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