Over-the-counter drug · NDA
LUMIFY Redness Reliever Eye Drops NDC 24208-537
brimonidine tartrate · Brimonidine tartrate .25 mg/mL · Solution/ drops · Ophthalmic · Bausch & Lomb Incorporated
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 24208-537-01 | 24208053701 | 1 AMPULE in 1 CARTON (24208-537-01) / .4 mL in 1 AMPULEMarketed from May 1, 2019 · Sample package | |
| 24208-537-05 | 24208053705 | 1 BOTTLE, DROPPER in 1 CARTON (24208-537-05) / 5 mL in 1 BOTTLE, DROPPERMarketed from Sep 25, 2020 | |
| 24208-537-08 | 24208053708 | 1 BOTTLE, DROPPER in 1 CARTON (24208-537-08) / 2.5 mL in 1 BOTTLE, DROPPERMarketed from Dec 22, 2017 | |
| 24208-537-10 | 24208053710 | 1 AMPULE in 1 CARTON (24208-537-10) / .4 mL in 1 AMPULEMarketed from May 1, 2019 · Sample package | |
| 24208-537-15 | 24208053715 | 2 BOTTLE, DROPPER in 1 CARTON (24208-537-15) / 7.5 mL in 1 BOTTLE, DROPPERMarketed from Apr 30, 2019 | |
| 24208-537-25 | 24208053725 | 1 BOTTLE, DROPPER in 1 CARTON (24208-537-25) / 7.5 mL in 1 BOTTLE, DROPPERMarketed from Dec 22, 2017 | |
| 24208-537-35 | 24208053735 | 1 BOTTLE, DROPPER in 1 CARTON (24208-537-35) / 3.5 mL in 1 BOTTLE, DROPPERMarketed from May 2, 2023 | |
| 24208-537-75 | 24208053775 | 1 BOTTLE, DROPPER in 1 CARTON (24208-537-75) / 7.5 mL in 1 BOTTLE, DROPPERMarketed from Dec 22, 2017 | |
| 24208-537-99 | 24208053799 | 1 BOTTLE, DROPPER in 1 CARTON (24208-537-99) / 2.5 mL in 1 BOTTLE, DROPPERMarketed from Dec 22, 2017 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- LUMIFY Redness Reliever Eye Drops
- Generic name (nonproprietary)
- brimonidine tartrate
- Active ingredients
- Brimonidine tartrate — .25 mg/mL
- Dosage form
- Solution/ drops
- Route
- Ophthalmic
- Labeler
- Bausch & Lomb Incorporated
- Product type
- Over-the-counter drug
- Marketing category
- NDA — New Drug ApplicationApplication NDA 208144
- Marketing start
- Listing expires
- Other FDA classes
- Adrenergic alpha-Agonists (Mechanism)
- Identifiers
- Product ID 24208-537_4e5af967-1d35-5b67-e063-6294a90a9296SPL ID 4e5af967-1d35-5b67-e063-6294a90a9296SPL set ID 022de945-0b26-40ae-8e88-d3fe2464d106RxCUI 1999016, 1999021UNII 4S9CL2DY2H
- Pharmacologic class
- alpha-Adrenergic Agonist
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Ophthalmic products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N424208053701followed by a unit qualifier and the quantityPackage 24208-0537-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Use relieves redness of the eye due to minor eye irritations
Excerpt only. Read the full label for complete information.