Muro 128 Ointment
NDC Package 24208-385-01
Package Information
Muro 128 (sodium chloride) ointment is a medication used to treat dryness inside the nose (nasal passages). This formulation utilizes a ointment delivery system. Marketed by Bausch & Lomb Incorporated, this product is identified by NDC 24208-385 and is authorized under FDA application M018.
Identification & Billing
- RxCUI: 1298435 - sodium chloride 5 % Ophthalmic Ointment
- RxCUI: 1298435 - sodium chloride 0.000855 MEQ/MG Ophthalmic Ointment
- RxCUI: 1298435 - NaCl 0.000855 MEQ/MG Ophthalmic Ointment
- RxCUI: 1298435 - NaCl 5 % Ophthalmic Ointment
- RxCUI: 1298435 - sodium chloride 50 MG (5 % ) Ophthalmic Ointment
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 24208 - Bausch & Lomb Incorporated
- 24208-385 - Muro 128
- 24208-385-01 - 1 TUBE in 1 CARTON / 1 g in 1 TUBE
- 24208-385 - Muro 128
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.
Other Available Packages
The following commercial packages are registered under the same Product NDC (24208-385). Click a package code to view its specific billing and regulatory data.
* 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 24208-385-01 identifies a specific commercial package of 1 tube in 1 carton / 1 g in 1 tube of Muro 128, a human over the counter drug labeled by Bausch & Lomb Incorporated. This ointment is formulated for ophthalmic use and contains sodium chloride 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 January 01, 2011. The current certification is valid through December 31, 2026.
What are the primary indications for this medication?
This product is used to treat dryness inside the nose (nasal passages). It helps add moisture inside the nose to dissolve and soften thick or crusty mucus. In babies and young children with stuffy noses who cannot blow their noses, using this product helps to make the mucus easier to remove with a nasal bulb syringe. This helps relieve stuffiness and makes breathing easier. This product contains a purified gentle salt solution (also called saline or sodium chloride solution). It does not contain any medication.
How is this Bausch & Lomb Incorporated product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 24208038501. 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.