Over-the-counter drug · UNAPPROVED DRUG OTHER
Premixed saline packets (Sodium chloride, sodium bicarbonate) NDC 83879-001
Sodium bicarbonate 700 mg/3000mg; Sodium chloride 2300 mg/3000mg · Granule, For solution · Nasal · Shenzhen Kerui lntl Trading Co., Ltd
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 83879-001-01 | 8387900010183879000101 | 100 BAG in 1 BOX (83879-001-01) / 3000 mg in 1 BAGMarketed from Dec 22, 2023 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Premixed saline packets
- Generic name (nonproprietary)
- sodium chloride, sodium bicarbonate
- Active ingredients
- Sodium bicarbonate — 700 mg/3000mgSodium chloride — 2300 mg/3000mg
- Dosage form
- Granule, For solution
- Route
- Nasal
- Labeler
- Shenzhen Kerui lntl Trading Co., LtdNDC labeler code 83879
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved drug (other)
- Marketing start
- Listing expires
- Other FDA classes
- Alkalinizing Activity (Mechanism)
- Identifiers
- Product ID 83879-001_2b42cc1e-2017-8753-e063-6394a90aad5fSPL ID 2b42cc1e-2017-8753-e063-6394a90aad5fSPL set ID 0d11e07b-c137-6efc-e063-6394a90a6bbaRxCUI 1542919UNII 8MDF5V39QO, 451W47IQ8X
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Nasal products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N483879000101followed by a unit qualifier and the quantityPackage 83879-0001-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Uses Relieve Nasal Passages From: ■Nasal symptoms from sinusitis, cold, flu ■Nasal allergies, dryness and Hay fever ■Sneezing, runny nose, nasal stuffiness ■lPost nasal drip and nasal congestion ■Removes nasal irritants (dust, pollen, animal dander, smoke etc) ■Promotes nasal and sinus drainage l■Moisturizes dry nasal passages ■Helps reduce swelling of nasal membranes
Excerpt only. Read the full label for complete information.
About NDC 83879-001
- What is NDC 83879-001?
- 83879-001 is the product NDC for Premixed saline packets, Sodium bicarbonate 700 mg/3000mg; Sodium chloride 2300 mg/3000mg granule, for solution, listed with the FDA by Shenzhen Kerui lntl Trading Co., Ltd. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Premixed saline packets (Sodium chloride, Sodium bicarbonate).
- What is the active ingredient?
- Sodium bicarbonate, Sodium chloride.
- Who is the labeler?
- Shenzhen Kerui lntl Trading Co., Ltd, NDC labeler code 83879. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Premixed saline packets?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.