Prescription drug · NDA
Fluorescein Sodium and Benoxinate Hydrochloride NDC 24208-734
Fluorescein sodium 2.6 mg/mL; Benoxinate hydrochloride 4.4 mg/mL · Solution/ drops · Ophthalmic · Bausch & Lomb Incorporated
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 24208-734-05 | 2420807340524208073405 | 1 BOTTLE, GLASS in 1 CARTON (24208-734-05) / 5 mL in 1 BOTTLE, GLASSMarketed from Mar 20, 2020 |
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)
- Fluorescein Sodium and Benoxinate Hydrochloride
- Generic name (nonproprietary)
- fluorescein sodium and benoxinate hydrochloride
- Active ingredients
- Fluorescein sodium — 2.6 mg/mLBenoxinate hydrochloride — 4.4 mg/mL
- Dosage form
- Solution/ drops
- Route
- Ophthalmic
- Labeler
- Bausch & Lomb IncorporatedNDC labeler code 24208
- Product type
- Prescription drug
- Marketing category
- NDA — New Drug ApplicationApplication NDA 211039
- Marketing start
- Listing expires
- Other FDA classes
- Dyes (Mechanism)
- Identifiers
- Product ID 24208-734_34f4eb14-b40e-1d6d-e063-6394a90a3e3bSPL ID 34f4eb14-b40e-1d6d-e063-6394a90a3e3bSPL set ID 1797c5ef-66c4-4cf8-b62d-b484242be2eeRxCUI 2287005UNII 93X55PE38X, 0VE4U49K15
- Pharmacologic class
- Diagnostic Dye
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
N424208073405followed by a unit qualifier and the quantityPackage 24208-0734-05. 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)
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. Fluorescein Sodium and Benoxinate Hydrochloride Ophthalmic Solution, 0.3%/0.4% is a combination of fluorescein sodium, a disclosing agent and benoxinate hydrochloride, a local ester anesthetic indicated for procedures in adult and pediatric patients requiring a disclosing agent in combination with a topical ophthalmic anesthetic. ( 1 )
Excerpt only. Read the full label for complete information.
About NDC 24208-734
- What is NDC 24208-734?
- 24208-734 is the product NDC for Fluorescein Sodium and Benoxinate Hydrochloride, Fluorescein sodium 2.6 mg/mL; Benoxinate hydrochloride 4.4 mg/mL solution/ drops, listed with the FDA by Bausch & Lomb Incorporated. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Fluorescein Sodium and Benoxinate Hydrochloride.
- What is the active ingredient?
- Fluorescein sodium, Benoxinate hydrochloride.
- Who is the labeler?
- Bausch & Lomb Incorporated, NDC labeler code 24208. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Fluorescein Sodium and Benoxinate Hydrochloride?
- 1 other product NDC are listed under this name. See all Fluorescein Sodium and Benoxinate Hydrochloride NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Fluorescein Sodium and Benoxinate Hydrochloride products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Fluorescein Sodium and Benoxinate Hydrochloride | Fluorescein sodium 2.6 mg/mL; Benoxinate hydrochloride 4.4 mg/mL | Solution/ dropsOphthalmic | Bausch & Lomb Americas Inc. | 82260-734 | 82260-0734-05 |
Other NDCs under NDA 211039
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Fluorescein Sodium and Benoxinate Hydrochloride | Fluorescein sodium 2.6 mg/mL; Benoxinate hydrochloride 4.4 mg/mL | Solution/ dropsOphthalmic | Bausch & Lomb Americas Inc. | 82260-734 |