Premixed Saline Packets Granule, For Solution
NDC Package 83879-001-01

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

Package Information

Premixed Saline Packets (sodium chloride, sodium bicarbonate) granules is adults and children 4 years and over:use 1-2 packets per 8 fl oz (240ml) up to every 2 hours as neededChildren under 4 years:Consult a physicianMixing one saline packet to 8 fl oz (240ml) of water creates an Isotonic saline solution (Hypertonic with 2 saline packets) that is PH balanced and preservative free.Isotonic solution1 saline packet per 8 fl oz (240 ml)Hypertonic solution2 saline packets per 8 fl oz (240 ml)An Isotonic solution has a gentle salt concentration of 9 mg of Sodium Chloride per ml of water, similar to your body's salt level. This formulation utilizes a granule, for solution delivery system. Marketed by Shenzhen Kerui Lnt�l Trading Co., Ltd, this product is identified by NDC 83879-001.

Identification & Billing

NDC Package Code
83879-001-01
Package Description
100 BAG in 1 BOX / 3000 mg in 1 BAG
Product Code
83879-001
11-Digit Billing Format
83879000101
RxNorm Crosswalk
  • RxCUI: 1542919 - sodium bicarbonate 700 MG / sodium chloride 2300 MG Powder for Nasal Solution
  • RxCUI: 1542919 - NaHCO3 700 MG / NaCl 2300 MG Powder for Nasal Solution

Clinical Specifications

Proprietary Name
Premixed Saline Packets
Non-Proprietary Name
Sodium Chloride, Sodium Bicarbonate
Substance Name
Sodium Bicarbonate; Sodium Chloride
Dosage Form
Granule, For Solution - A small medicinal particle or grain made available in its more stable dry form, to be reconstituted with solvent just before dispensing; the granules are so prepared to contain not only the medicinal agent, but the colorants, flavorants, and any other desired pharmaceutic ingredient.
Administration Route
Nasal - Administration to the nose; administered by way of the nose.
Active Ingredient(s)
Pharmacologic Class
Alkalinizing Activity - [MoA] (Mechanism of Action)
Usage Information
Adults and children 4 years and over:use 1-2 packets per 8 fl oz (240ml) up to every 2 hours as neededChildren under 4 years:Consult a physicianMixing one saline packet to 8 fl oz (240ml) of water creates an Isotonic saline solution (Hypertonic with 2 saline packets) that is PH balanced and preservative free.Isotonic solution1 saline packet per 8 fl oz (240 ml)Hypertonic solution2 saline packets per 8 fl oz (240 ml)An Isotonic solution has a gentle salt concentration of 9 mg of Sodium Chloride per ml of water, similar to your body's salt level. It can be more comfortable for some initially than a stronger Hypertonic solution.A Hypertonic solution has a higher salt concentration, akin to ocean water's salt content.

Regulatory & Marketing

Labeler Name
Shenzhen Kerui Lnt�l Trading Co., Ltd
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
12-22-2023
Listing Expiration
12-31-2026
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 83879-001-01 identifies a specific commercial package of 100 bag in 1 box / 3000 mg in 1 bag of Premixed Saline Packets, a human over the counter drug labeled by Shenzhen Kerui Lnt�l Trading Co., Ltd. This granule, for solution is formulated for nasal use and contains sodium bicarbonate; 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 Shenzhen Kerui Lnt�l Trading Co., Ltd on December 22, 2023. The current certification is valid through December 31, 2026.

How is this Shenzhen Kerui Lnt�l Trading Co., Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 83879000101. 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)
83879-001-01
11-Digit CMS (5-4-2)
83879-0001-01

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