Device - Nebuclear Md Hand-held Rubber Bulb Nebulizer Solution
NDC Package 73117-509-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Device - Nebuclear Md Hand-held Rubber Bulb Nebulizer (device - hand-held rubber bulb nebulizer) solution is connect bulb to solutions cup.Open top of cup, add approved Bronchodilator, close solutions cup.Squeeze bulb vigorously so visible vapor comes from the top.Breathe in slowly until approved Bronchodilator is gone.Disconnect bulb and follow Cleaning Instructions. This formulation utilizes a solution delivery system. Marketed by Blue Echo Care Llc, this product is identified by NDC 73117-509 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
73117-509-01
Package Description
1 mL in 1 BOTTLE, SPRAY
Product Code
11-Digit Billing Format
73117050901

Clinical Specifications

Proprietary Name
Device - Nebuclear Md Hand-held Rubber Bulb Nebulizer
Non-Proprietary Name
Device - Hand-held Rubber Bulb Nebulizer
Substance Name
Racepinephrine Hydrochloride
Dosage Form
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route
Respiratory (inhalation) - Administration within the respiratory tract by inhaling orally or nasally for local or systemic effect.
Usage Information
Connect bulb to solutions cup.Open top of cup, add approved Bronchodilator, close solutions cup.Squeeze bulb vigorously so visible vapor comes from the top.Breathe in slowly until approved Bronchodilator is gone.Disconnect bulb and follow Cleaning Instructions.

Regulatory & Marketing

Labeler Name
Blue Echo Care Llc
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
11-18-2025
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

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 73117-509-01 identifies a specific commercial package of 1 ml in 1 bottle, spray of Device - Nebuclear Md Hand-held Rubber Bulb Nebulizer, a human over the counter drug labeled by Blue Echo Care Llc. This solution is formulated for respiratory (inhalation) use and contains racepinephrine hydrochloride 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 November 18, 2025. The current certification is valid through December 31, 2027.

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: 73117050901. 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)
73117-509-01
11-Digit CMS (5-4-2)
73117-0509-01

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