Fluorescein Sodium And Benoxinate Hydrochloride Solution/ Drops
NDC Package 24208-734-05
Package Information
Fluorescein Sodium And Benoxinate Hydrochloride solution/ dropses is fluorescein Sodium and Benoxinate Hydrochloride Ophthalmic Solution, 0.3%/0.4% is indicated for ophthalmic procedures in adult and pediatric patients requiring a disclosing agent in combination with a topical ophthalmic anesthetic agent. This formulation utilizes a solution/ drops delivery system. Marketed by Bausch & Lomb Incorporated, this product is identified by NDC 24208-734 and is authorized under FDA application NDA211039.
Identification & Billing
- RxCUI: 2287005 - benoxinate HCl 0.4 % / fluorescein sodium 0.3 % Ophthalmic Solution
- RxCUI: 2287005 - benoxinate hydrochloride 4 MG/ML / fluorescein sodium 3 MG/ML Ophthalmic Solution
- RxCUI: 2287005 - benoxinate hydrochloride 0.4 % / fluorescein sodium 0.3 % Ophthalmic Drops
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 24208 - Bausch & Lomb Incorporated
- 24208-734 - Fluorescein Sodium And Benoxinate Hydrochloride
- 24208-734-05 - 1 BOTTLE, GLASS in 1 CARTON / 5 mL in 1 BOTTLE, GLASS
- 24208-734 - Fluorescein Sodium And Benoxinate Hydrochloride
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 24208-734-05 identifies a specific commercial package of 1 bottle, glass in 1 carton / 5 ml in 1 bottle, glass of Fluorescein Sodium And Benoxinate Hydrochloride, a human prescription drug labeled by Bausch & Lomb Incorporated. This solution/ drops is formulated for ophthalmic use and contains benoxinate hydrochloride; fluorescein sodium as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Bausch & Lomb Incorporated on March 20, 2020. The current certification is valid through December 31, 2026.
How is this Bausch & Lomb Incorporated product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 24208073405. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.