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Fluorescein Sodium and Benoxinate Hydrochloride

NDC 24208-734, Fluorescein Sodium and Benoxinate Hydrochloride, solution/ drops, from Bausch & Lomb Incorporated.

Product NDC
24208-734
Status
Listed
Labeler
Bausch & Lomb Incorporated
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA211039
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/24208-734 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FLUORESCEIN SODIUM2.6 mg/mL
  • BENOXINATE HYDROCHLORIDE4.4 mg/mL

Pharmacologic classes

Diagnostic Dye [EPC]; Dyes [MoA]

Package NDCNDC-11Package
24208-734-05242080734051 BOTTLE, GLASS in 1 CARTON (24208-734-05) / 5 mL in 1 BOTTLE, GLASS

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1797c5ef-66c4-4cf8-b62d-b484242be2ee

Use it

Look up 24208-734 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/24208-734 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 24208-734. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.