Fluorescein Sodium and Benoxinate Hydrochloride is a Ophthalmic Solution/ Drops in the Human Prescription Drug category. It is labeled and distributed by Bausch & Lomb Incorporated. The primary component is Benoxinate Hydrochloride; Fluorescein Sodium.
| Product ID | 24208-732_71938df7-eb38-4a21-9267-ea4b355b8c1e |
| NDC | 24208-732 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Fluorescein Sodium and Benoxinate Hydrochloride |
| Generic Name | Fluorescein Sodium And Benoxinate Hydrochloride |
| Dosage Form | Solution/ Drops |
| Route of Administration | OPHTHALMIC |
| Marketing Start Date | 1995-01-01 |
| Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
| Labeler Name | Bausch & Lomb Incorporated |
| Substance Name | BENOXINATE HYDROCHLORIDE; FLUORESCEIN SODIUM |
| Active Ingredient Strength | 4 mg/mL; mg/mL |
| Pharm Classes | Diagnostic Dye [EPC],Dyes [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 1995-01-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | Unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1995-01-01 |
| Ingredient | Strength |
|---|---|
| BENOXINATE HYDROCHLORIDE | 4 mg/mL |
| SPL SET ID: | 1c5a620f-7083-4fee-99e2-c9380541c368 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 24208-732 | Fluorescein Sodium and Benoxinate Hydrochloride | Fluorescein Sodium and Benoxinate Hydrochloride |
| 24208-734 | Fluorescein Sodium and Benoxinate Hydrochloride | Fluorescein Sodium and Benoxinate Hydrochloride |
| 68682-732 | Fluorescein Sodium and Benoxinate Hydrochloride | Fluorescein Sodium and Benoxinate Hydrochloride |
| 59390-206 | ALTAFLUOR | Fluorescein Sodium and Benoxinate Hydrochloride |
| 59390-218 | ALTAFLUOR | Fluorescein Sodium and Benoxinate Hydrochloride |
| 17478-640 | FLURESS | Fluorescein Sodium and Benoxinate Hydrochloride |