CVS Sodium Chloride, Sodium Bicarbonate Kit
by CVS Pharmacy, Inc. · 1 KIT in 1 PACKAGE (69842-349-30) * 30 PACKET in 1 KIT / 3000 mg in 1 PACKET (69842-324-01)
NDC 69842-0349-30
🏷️ FDA NDC (as labeled)
69842-349-30
billing pads the product segment with a zero
This package
Contains3000 mg in 1 packet
Pack sizes3 compare ↓
OTC
On market
Non-controlled
🗂️ Data synced 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
FDA NDC (as labeled)
69842-349-30
Product NDC
69842-349
11-digit billing NDC
69842034930
RxCUI
1542919
SPL Set ID
a782735a-862b-7173-e053-2995a90ad85d
DEA schedule
Non-controlled
Marketing category
UNAPPROVED DRUG OTHER
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2016-03-25
Dosage form
KIT
Why two NDCs?
The FDA registers this code as 69842-349-30 — 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 → 69842-0349-30. 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.
🏷️ 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.
🏭 Manufacturer & labeler
LabelerCVS Pharmacy, Inc.
Labeler code69842
First marketedMar 2016
Product typeHuman Otc Drug
Portfolio128 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.
🩺 Clinical
🧪 What is this product?
This is an unapproved over-the-counter kit containing sodium chloride and sodium bicarbonate. Sodium chloride (salt) is commonly used in saline solutions for nasal irrigation and wound cleansing. Sodium bicarbonate (baking soda) is typically used as an antacid to relieve heartburn and indigestion. This kit product is not approved by the FDA, so consult product labeling or a healthcare provider for specific uses and directions.
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.
💬 Questions about Sodium Chloride, Sodium Bicarbonate?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
🧪 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.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.
💲 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
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.
🔁 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 Pharmacy 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 | — |
| Cvsthis 69842-0349-30 | 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.
⏳ Availability & generic status
🏛️
2016
On the market since
Mar 2016
📍
2026
Currently FDA-listed
10 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.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 69842-0349-10 | 1 KIT in 1 KIT (69842-349-10) * 10 PACKET in 1 KIT / 3000 mg in 1 PACKET (69842-324-01) | 2016-03-25 | Active |
| 69842-0349-20 | 1 KIT in 1 KIT (69842-349-20) * 30 PACKET in 1 KIT / 3000 mg in 1 PACKET (69842-324-01) | 2015-07-01 | Active |
| 69842-0349-30 You're viewing this | 1 KIT in 1 PACKAGE (69842-349-30) * 30 PACKET in 1 KIT / 3000 mg in 1 PACKET (69842-324-01) | 2013-04-01 | Active |
Pack size FAQ
What quantity is in NDC 69842-0349-30?
NDC 69842-0349-30 is listed by the FDA — 1 kit in 1 package * 30 packet in 1 kit / 3000 mg in 1 packet.
What NDC number is used to bill for this package of CVS Sodium Chloride, Sodium Bicarbonate Kit?
Bill NDC 69842-0349-30 — the 11-digit billing format is 69842034930. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.
🧭 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 | — Not published for this NDC No photo available yet for this listing. |
| 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 FDA registers it as 69842-349-30, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 69842-0349-30, written without dashes as 69842034930. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 69842-0349-30, the first segment (69842) is the labeler code FDA assigned to CVS Pharmacy, Inc.; the middle segment (0349) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (30) identifies this exact package size and type. Together they name one specific package of one specific product.
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 CVS Pharmacy, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 2 other package presentations of this same product, including 1 kit (69842-0349-10), 1 kit (69842-0349-20). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
CVS Pharmacy, Inc. 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.
📄 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
🎯 Indications and Usage ▾
Uses Temporarily relieves symptoms associated with sinusitis, cold, flu or allergies: -Sneezing -Runny nose -Nasal stuffiness -Post nasal drip -Removes inhaled irritants (dust, pollen) -Promotes 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 - 1 packet per 4 fl. oz (120 mL) up to every 2 hours as needed Children under 4 years: Consult a physician See enclosed instruction sheet for complete instructions and proper use
⚠️ Warnings ▾
Warnings Stop use and ask a doctor if washing is uncomfortable or symptoms are not reduced. 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. When using this product: Use by only one person Wash with soap and water after each use Top rack of dishwasher safe Do not heat in microwave
🧪 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
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 ↗
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.