Nebuclear Md Liquid
NDC Package 73117-520-19

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Nebuclear Md (saline) liquids is a medication used to treat dryness inside the nose (nasal passages). This formulation utilizes a liquid delivery system. Marketed by Blue Echo Care Llc, this product is identified by NDC 73117-520 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
73117-520-19
Package Description
20 mg in 1 BOX
Product Code
73117-520
11-Digit Billing Format
73117052019

Clinical Specifications

Proprietary Name
Nebuclear Md
Non-Proprietary Name
Saline
Substance Name
Sodium Chloride
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Respiratory (inhalation) - Administration within the respiratory tract by inhaling orally or nasally for local or systemic effect.
Active Ingredient(s)
SODIUM CHLORIDE 9 mg/9mg
Usage Information
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.

Regulatory & Marketing

Labeler Name
Blue Echo Care Llc
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-01-2025
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 73117-520-19 identifies a specific commercial package of 20 mg in 1 box of Nebuclear Md, a human over the counter drug labeled by Blue Echo Care Llc. This liquid is formulated for respiratory (inhalation) 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 Blue Echo Care Llc on September 01, 2025. The current certification is valid through December 31, 2027.

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 Blue Echo Care Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 73117052019. 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:

10-Digit Format (5-3-2)
73117-520-19
11-Digit CMS (5-4-2)
73117-0520-19

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.