Search by Drug Name or NDC
NDC 24208-0537-01 LUMIFY Redness Reliever Eye Drops 0.25 mg/mL Details
LUMIFY Redness Reliever Eye Drops 0.25 mg/mL
LUMIFY Redness Reliever Eye Drops is a OPHTHALMIC SOLUTION/ DROPS in the HUMAN OTC DRUG category. It is labeled and distributed by Bausch & Lomb Incorporated. The primary component is BRIMONIDINE TARTRATE.
MedlinePlus Drug Summary
Ophthalmic brimonidine is used to lower pressure in the eyes in patients who have glaucoma (high pressure in the eyes that may damage nerves and cause vision loss) and ocular hypertension (pressure in the eyes that is higher than normal but not high enough to cause vision loss). Brimonidine is in a class of drugs called alpha adrenergic agonists. Brimonidine works by decreasing the amount of fluid in the eyes.
Related Packages: 24208-0537-01Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Brimonidine Ophthalmic
Product Information
| NDC | 24208-0537 |
|---|---|
| Product ID | 24208-537_31470602-4f2f-4341-a0b3-ddf14278df7e |
| Associated GPIs | 86602020102002 |
| GCN Sequence Number | 078056 |
| GCN Sequence Number Description | brimonidine tartrate DROPS 0.025 % OPHTHALMIC |
| HIC3 | Q6D |
| HIC3 Description | EYE VASOCONSTRICTORS (OTC ONLY) |
| GCN | 44289 |
| HICL Sequence Number | 011786 |
| HICL Sequence Number Description | BRIMONIDINE TARTRATE |
| Brand/Generic | Brand |
| Proprietary Name | LUMIFY Redness Reliever Eye Drops |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | BRIMONIDINE TARTRATE |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | SOLUTION/ DROPS |
| Route | OPHTHALMIC |
| Active Ingredient Strength | 0.25 |
| Active Ingredient Units | mg/mL |
| Substance Name | BRIMONIDINE TARTRATE |
| Labeler Name | Bausch & Lomb Incorporated |
| Pharmaceutical Class | Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC] |
| DEA Schedule | n/a |
| Marketing Category | NDA |
| Application Number | NDA208144 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 24208-0537-01 (24208053701)
| NDC Package Code | 24208-537-01 |
|---|---|
| Billing NDC | 24208053701 |
| Package | 1 AMPULE in 1 CARTON (24208-537-01) / .4 mL in 1 AMPULE |
| Marketing Start Date | 2019-05-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |