# Fluorescein Sodium and Benoxinate Hydrochloride

NDC: 24208-734
Generic name: Fluorescein Sodium and Benoxinate Hydrochloride
Labeler / Manufacturer: Bausch & Lomb Incorporated
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SOLUTION/ DROPS
Routes: OPHTHALMIC
Marketing started: 20200320

FDA application: NDA211039

## Active ingredients

- BENOXINATE HYDROCHLORIDE: 4.4 mg/mL
- FLUORESCEIN SODIUM: 2.6 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"24208-734"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=24208-734
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1797c5ef-66c4-4cf8-b62d-b484242be2ee