Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.
Soft Tip Squeeze bottle Sinus Wash Good Neighbor Pharmacy SODIUM BICARBONATE, SODIUM CHLORIDE Kit — NDC 24385-121-01 (Billing 24385-0121-01)
by AMERISOURCE BEGEN · 1 KIT in 1 KIT * 3000 mg in 1 PACKET
This is a package of Soft Tip Squeeze bottle Sinus Wash Good Neighbor Pharmacy SODIUM BICARBONATE, SODIUM CHLORIDE Kit from AMERISOURCE BEGEN, marketed since Jan 2022 and currently FDA-listed. It is this product's only package size.
NDC 24385-0121-01
🏷️ FDA NDC (as labeled)
24385-121-01
billing pads the product segment with a zero
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
FDA NDC (as labeled)
24385-121-01
Product NDC
24385-121
11-digit billing NDC
24385012101
RxCUI
1542919
SPL Set ID
e215964e-461f-ee52-e053-2995a90aac95
DEA schedule
Non-controlled
Marketing category
UNAPPROVED DRUG OTHER
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2022-01-09
Route
NASAL
Dosage form
KIT
Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification
GPI-14
43993002950920
GPI class
GNP Triacting Night Time Child
Quick answers
- GPI-14 (Medi-Span): 43993002950920
- RxCUI (RxNorm): 1542919
Why two NDCs?
The FDA registers this code as 24385-121-01 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 24385-0121-01. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
RxNorm drug class
This medicine belongs to the Salt solutions class.
Drug family (ATC)
Salt solutions, Electrolyte solutions
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.
- RxClass (NLM) · catalog refreshed Oct 1, 2026
Clinical
🧪 What is this product?
This is a nasal rinse kit supplied as a squeeze bottle containing sodium bicarbonate and sodium chloride. These salts are commonly used in saline nasal irrigation products to help rinse and clear the nasal passages. The kit is an unapproved over-the-counter drug product and does not have an FDA-approved application.
Patient education
Supplement & herbal interactions
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
💬 Questions about SODIUM BICARBONATE, SODIUM CHLORIDE?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
Pricing
A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.
| Price system | Per each | Per package |
|---|---|---|
| Retail pharmacies payNADAC · weekly | Not in the retail survey — common for institutional, discontinued, or low-volume packs. | |
| Medicaid paysCMS SDUD · 12 mo | No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data. | |
| Medicare drug plans payPart D · quarterly | No Part D plan price is available for this NDC in our data. | |
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 2, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 24385-0121-01 You're viewing this Main listing | 1 KIT in 1 KIT * 3000 mg in 1 PACKET | 2022-01-09 | — | Active |
Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Well at Walgreens 00363-0504-30 | Walgreen | 1 kit | — | — | FDA listed | — |
| Well at Walgreens 700 mg/3000mg; 2300 mg/3000mg 00363-0801-10 | Walgreen | 100 packets | — | — | FDA listed | — |
| Well at Walgreens 700 mg/3000mg; 2300 mg/3000mg 00363-0802-00 | Walgreen | 3000 mg | — | — | FDA listed | — |
| Walgreens Sinus Wash Squeeze Bottle Kit 00363-1405-31 | Walgreen | 1 kit | — | — | FDA listed | — |
| Soft Tip Neti Pot Sinus Wash Rite Aid 11822-0427-01 | RITE | 1 kit | — | — | FDA listed | — |
| Soft Tip Squeeze bottle Sinus Wash Rite Aid 11822-0429-01 | RITE | 1 kit | — | — | FDA listed | — |
| Sinus Wash Pre Mixed Ready to Use Rite Aid 11822-0472-08 | RITE | 1 kit | — | — | FDA listed | — |
| Sinus Wash Packet 700 mg/3000mg; 2300 mg/3000mg 11822-0484-00 | RITE | 100 packets | — | — | FDA listed | — |
| Sinus Wash Squeeze Bottle Kit 21130-0972-01 | Better | 1 kit | — | — | FDA listed | — |
| Sinus Wash Packet 700 mg/3000mg; 2300 mg/3000mg 21130-0984-50 | BETTER | 50 packets | — | — | FDA listed | — |
| Soft Tip Squeeze bottle Sinus Wash Good Neighbor Pharmacythis 24385-0121-01 | AMERISOURCE | 1 kit | — | — | FDA listed | — |
| Sinus Wash Saline Packets Good Neighbor Pharmacy 24385-0267-10 | AMERISOURCE | 1 kit | — | — | FDA listed | — |
| Soft Tip Neti Pot Good Neighbor Pharmacy 24385-0451-01 | AMERISOURCE | 1 kit | — | — | FDA listed | — |
| Soft Tip Neti Pot Sinus wash CareOne 41520-0929-30 | FOODHOLD | 1 kit | — | — | FDA listed | — |
| All natural Saline Packets CareOne 700 mg/3000mg; 2300 mg/3000mg 41520-0938-50 | FOODHOLD | 50 packets | — | — | FDA listed | — |
| SinuCleanse 700 mg/3000mg; 2300 mg/3000mg 42829-0401-01 | ASCENT | 3000 mg | — | — | FDA listed | — |
| SinuCleanse Neti-Pot 42829-0402-30 | ASCENT | 1 kit | — | — | FDA listed | — |
| SinuCleanse Squeeze 42829-0405-30 | ASCENT | 1 kit | — | — | FDA listed | — |
| SinuCleanse Micro-Filtered Nasal Wash System 42829-0406-30 | ASCENT | 1 kit | — | — | FDA listed | — |
| SinuCleanse 22.2 mg/100mg; 77.8 mg/100mg 42829-0408-60 | ASCENT | 60 packets | — | — | FDA listed | — |
| Rexall Sinus Wash System Soft Tip Squeeze bottle 55910-0919-20 | Dolgencorp, | 1 kit | — | — | FDA listed | — |
| Cvs 22.8 mg/100mg; 77.8 mg/100mg 59779-0408-01 | CVS | 3000 mg | — | — | FDA listed | — |
| Soft Tip Neti Pot Easy to use Sinus Relief Premier Value 68016-0451-01 | Premier | 1 kit | — | — | FDA listed | — |
| Soft Tip Squeeze bottle Sinus Wash Premier Value 68016-0452-01 | Premier | 1 kit | — | — | Discontinued | — |
| Cvs 69842-0349-10 | CVS | 1 kit | — | — | FDA listed | — |
| Cvs 69842-0453-10 | CVS | 1 kit | — | — | FDA listed | — |
| Leader Sinus Wash Saline Refill Packets 700 mg/3g; 2300 mg/3g 70000-0270-01 | Cardinal | 30 packets | — | — | FDA listed | — |
| Soft Tip Neti Pot Sinus wash Meijer 79481-0500-01 | Meijer, | 1 kit | — | — | FDA listed | — |
| Soft Tip Squeeze bottle Sinus Wash Meijer 79481-0501-01 | Meijer, | 1 kit | — | — | FDA listed | — |
| Sinus Wash Saline Refills Meijer 700 mg/3000mg; 2300 mg/3000mg 79481-0502-02 | Meijer, | 100 packets | — | — | FDA listed | — |
| Premixed saline packets 700 mg/3000mg; 2300 mg/3000mg 83879-0001-01 | Shenzhen | 3000 mg | — | — | FDA listed | — |
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Sep 3, 2026
- CMS NADAC weekly file
Availability & generic status
🏛️
2022
On the market since
Jan 2022
📍
2026
Currently FDA-listed
4 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found
We did not find an FDA-approved generic match for this exact strength, form and route.
Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.
- FDA Orange Book · refreshed Sep 3, 2026
Inactive Ingredients / Excipients
Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.
From the label’s inactive-ingredient sectionInactive Ingredients None
This is label-wide narrative text, not a normalized exact-product ingredient list. A label can cover multiple strengths or packages.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured
IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.- FDA label on DailyMed · label index refreshed Oct 1, 2026
- FDA openFDA NDC Directory · synced Oct 1, 2026
Inactive ingredient FAQ
Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.
Manufacturer & labeler
LabelerAMERISOURCE BEGEN
Labeler code24385
First marketedJan 2022
Product typeHuman Otc Drug
Portfolio3 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
FDA label — Drug Facts FDA SPL
The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage
⏱️ Dosage and Administration
⚠️ Warnings
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
📄 Keep Out of Reach of Children
📄 Other Information
📄 Package Label / Principal Display Panel
🎯 Indications and Usage ▾
Uses Temporarily relieves symptoms associated with sinusitis, cold, flu or allergies -Sneezing -Nasal Stuffiness -Runny nose -Post nasal drip Removes inhaled irritants (dust, pollen) Removes nasal and sinus drainage Helps reduce swelling of nasal membranes Moisturizes dry nasal passages
⏱️ Dosage and Administration ▾
Directions Adults and children 4 years and over: Use 1-2 packets per 8 fl oz (240 mL) up to every 2 hours as needed. Children under 4 years: Consult a physician See enclosed instruction sheet for complete directions and proper use.
⚠️ Warnings ▾
Warnings Stop use and ask a doctor if washing is uncomfortable or symptoms are not relieved. Do not use unfiltered tap water. see instructions inside box for proper water sources Do not use if nasal passages are completely blocked or if you have an ear infection or blocked ears.
🧪 Active Ingredient ▾
Active ingredients (in each packet) Sodium Bicarbonate USP (700 mg) Sodium Chloride USP (2300 mg)
🧪 Inactive Ingredients ▾
Inactive Ingredients None
🎯 Purpose ▾
Purpose Nasal Wash
📄 Keep Out of Reach of Children ▾
Keep out of reach of children
📄 Other Information ▾
Other Information -Inspect saline packets for integrity -Do not use saline packets if open or torn -Protect saline packets from excessive heat and moisture -See saline packets or box for lot number and expiration date Questions? 1-888-547-5492
📄 Package Label / Principal Display Panel ▾
1
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
Reported adverse events (FAERS)
Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Soft Tip Squeeze bottle Sinus Wash Good Neighbor Pharmacy (this brand).
Top reported reactions
Reporter sex
Male · 50%
Female · 50%
Serious outcomes
Reports over time (by year) — tap or hover for the count & year
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.
About this NDC listing & data coverage
Over-the-counter (OTC) product
Marketed without an FDA application
Kit / multi-component package
Listed without an FDA application
This product's marketing category indicates it is marketed without an approved FDA application (no NDA, ANDA, or BLA on file). Having an NDC does not by itself establish FDA approval — the NDC Directory is a listing system, not an approval decision. Approval-linked data such as Orange Book therapeutic-equivalence ratings therefore does not apply.
Kit / multi-component package
This NDC identifies a kit — a package containing more than one component. Structured data (pricing, ingredients, equivalents) is often reported per component rather than for the kit NDC itself, which can make this page look thinner than the components' own pages.
What data is (and isn’t) available for this NDC — tap to expand
| NDC identity (package / product / labeler codes) | ✓ Available |
| Labeler | ✓ Available |
| Product & package description | ✓ Available |
| Marketing category & status | ✓ Available |
| Active ingredient / dosage form / route | ✓ Available |
| FDA label (SPL via DailyMed) | ✓ Available |
| Package photos | ✓ Available |
| Inactive ingredients (structured) | ✓ Available |
| NADAC pharmacy acquisition price (CMS) | — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey. |
| Orange Book / therapeutic-equivalence data | — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope. |
| HCPCS J-code billing crosswalk | — Not published for this NDC Most self-administered / retail products have no J-code — that is normal. |
| Medicaid utilization (CMS SDUD) | — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold. |
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.
Questions about this listing
Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Unapproved Drug Other". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by AMERISOURCE BEGEN. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
AMERISOURCE BEGEN is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
For educational and professional reference only — not medical advice. Pricing reflects published
NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.