0.9% Sodium Chloride Injection, Solution
NDC Package 51662-1609-1
Package Information
0.9% Sodium Chloride injection is a medication used to treat dryness inside the nose (nasal passages). This formulation utilizes a injection, solution delivery system. Marketed by Hf Acquisition Co Llc, Dba Healthfirst, this product is identified by NDC 51662-1609 and is authorized under FDA application ANDA207956.
Identification & Billing
- RxCUI: 1807634 - sodium chloride 0.9 % in 500 ML Injection
- RxCUI: 1807634 - 500 ML sodium chloride 9 MG/ML Injection
- RxCUI: 1807634 - 500 ML NaCl 9 MG/ML Injection
- RxCUI: 1807634 - sodium chloride 0.9 % per 500 ML Injection
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 51662 - Hf Acquisition Co Llc, Dba Healthfirst
- 51662-1609 - 0.9% Sodium Chloride
- 51662-1609-1 - 500 mL in 1 BAG
- 51662-1609 - 0.9% Sodium Chloride
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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 51662-1609-1 identifies a specific commercial package of 500 ml in 1 bag of 0.9% Sodium Chloride, a human prescription drug labeled by Hf Acquisition Co Llc, Dba Healthfirst. This injection, solution is formulated for intravenous 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 Hf Acquisition Co Llc, Dba Healthfirst on July 31, 2022. 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 Hf Acquisition Co Llc, Dba Healthfirst product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 51662160901. 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 Package segment to maintain the 5-4-2 structure.