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CVS Sodium Chloride, Sodium Bicarbonate Kit — NDC 69842-349-10 (Billing 69842-0349-10)

by CVS Pharmacy, Inc. · 1 KIT in 1 KIT * 10 PACKET in 1 KIT / 3000 mg in 1 PACKET

This is a package of CVS Sodium Chloride, Sodium Bicarbonate Kit from CVS Pharmacy, Inc., marketed since Mar 2016 and currently FDA-listed. It is the main listing for this product, which comes in 3 package sizes.

NDC 69842-0349-10
🏷️ FDA NDC (as labeled) 69842-349-10 billing pads the product segment with a zero
This package
Contains3000 mg in 1 packet Pack sizes3 compare ↓
Main listing for product 69842-349 · Also comes in: 3000 mg 69842-349-20 3000 mg 69842-349-30
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ 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 →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

NDC database record

One package, one record: these facts belong to NDC 69842-349-10 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
69842 labeler · 349 product · 10 package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 6984234910 5
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 69842-349-10
Product NDC 69842-349
11-digit billing NDC 69842034910
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
Quick answers
  • RxCUI (RxNorm): 1542919
Why two NDCs? The FDA registers this code as 69842-349-10 — 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 → 69842-0349-10. 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.

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.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
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.

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 systemPer eachPer 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.
Try another pack size: 3000 mg 3000 mg
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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
69842-0349-10 You're viewing this Main listing 1 KIT in 1 KIT * 10 PACKET in 1 KIT / 3000 mg in 1 PACKET 2016-03-25 — Active
69842-0349-20 69842-349-20 1 KIT in 1 KIT * 30 PACKET in 1 KIT / 3000 mg in 1 PACKET 2015-07-01 — Active
69842-0349-30 69842-349-30 1 KIT in 1 PACKAGE * 30 PACKET in 1 KIT / 3000 mg in 1 PACKET 2013-04-01 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 kit in 1 kit * 10 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?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice 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 69842-0349-10 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.

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.

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.

Manufacturer & labeler

LabelerCVS Pharmacy, Inc.
Labeler code69842
First marketedMar 2016
Product typeHuman Otc Drug
Portfolio129 products on file

More NDCs from CVS Pharmacy, Inc. labeler code 69842

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 label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Very long sections are excerpted here and marked; the full text is on DailyMed (linked in the sources below). 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 📄 Questions or Comments 📖 Instructions for Use 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 39 words ▾

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 43 words ▾

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 76 words ▾

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 15 words ▾

Active ingredients (in each packet) Sodium Bicarbonate USP 700 mg Sodium Chloride USP 2300 mg

🧪 Inactive Ingredients 3 words ▾

Inactive ingredients: none

🎯 Purpose 3 words ▾

Purpose Nasal Wash

📄 Keep Out of Reach of Children 6 words ▾

Keep out of reach of children

📄 Other Information 35 words ▾

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 or Comments 2 words ▾

Questions? 1-888-547-5492

📖 Instructions for Use ~3 min read ▾

*IMPORTANT NOTE Do not sinus wash with unfiltered tap water. Use either distilled, or sterile, or filtered (using a filter with an absolute pore size of 1 micron or smaller) or previously boiled water (boil water 1 minute or 3 minutes if at elevations above 6,500 feet then allow to cool to body temperature). Sinus Wash Compact Neti Pot Instructions Read through entire instruction sheet before using for the first time.

DO NOT SINUS WASH WITH UNFILTERED TAP WATER . See important note* for proper water sources . Warning : Do not rinse if nasal passages are completely blocked or if you have an ear infection or blocked ears.

Should I use an Isotonic or Hypertonic Solution? Any Sinus Wash Device can be used with the enclosed Saline packets to make either an Isotonic or Hypertonic solution. Check with the guide below or consult with your physician for best use.

Isotonic Solution 1/2 Saline Packet per 4 fl oz. (120 mL) Hypertonic Solution 1 Saline Packets per 4 fl oz. (120 mL) An Isotonic solution creates a mild, less concentrated salt solution of 9 mg of Sodium Chloride per mL of water, which has a similar salt concentration of your body and may be more comfortable to use for some people initially than a more concentrated Hypertonic solution.

A Hypertonic solution creates a higher, more concentrated salt solution which is similar to the salt content of ocean water. What is the Sinus Wash System? The Sinus Wash System is an all natural and medically proven method for relieving allergies, nasal congestion, discomfort caused by dry air, sinus infections, rhinitis of pregnancy and soothing irritated nasal passages.

It gently washes away mucus buildup from the nose and improves breathing. Because it is gentle, the system can be used up to every 2 hours as needed. Some people use it as routinely as they brush their teeth while others use it only on days when they need it.

ACP No. 99-40330-205-00 Instructions for Use of the Compact Neti Pot: Directions & Dosage: Read through entire section before using for the first time. 1.

Pour the pre-mixed saline dry ingredients into the Compact Neti Pot. First-time users should start with 1/2 packet of the saline dry ingredients. As you become more accustomed to the system, work up to using 1 full packet.

Additional packets may be purchased from your nearest pharmacy. 2. Fill the pot to the 4 oz. line with proper water*.

This makes 1/2 cup (4 oz.) of solution. 3. Stir thoroughly until the dry ingredients have completely dissolved.

4. Proper head position allows solution to flow through the nose by gravity. •Lean over the sink with your head bent down so you are looking directly into the basin. Holding the Neti Pot in your right hand, gently insert the spout into your right nostril so that it forms a comfortable seal. • Rotate your head so that the right nostril is directly above the left.

The forehead should remain higher than the chin. Raise the Neti Pot so that the solution enters the right nostril. In a few moments, the solution will begin to drain out the left nostril into the sink.

Do not inhale or “snort” solution into the nose – breathe through your mouth. 5. When the Neti Pot is empty, exhale through both nostrils to clear them of excess mucus and solution.

Gently blow your nose into a tissue. 6. Repeat the procedure on the left nostril.

7. Thoroughly rinse the Neti Pot after each use with water that has been distilled, sterilized, filtered or previously boiled and leave the pot open to air dry completely. The Compact Neti Pot is top-rack dishwasher safe.

Hints for a more comfortable nasal wash: • Begin using the Sinus Wash System slowly – especially with children. A full pot of solution on each side is not necessary to receive the full benefit. • If the solution is too warm or too cold, the nasal wash will be uncomfortable. • If stinging or irritation occurs, try using 1/2 packet of dry ingredients per pot. Gradually work up to using the solution at full strength using 1 full packet per pot.

D… [Excerpted — this section continues on DailyMed.]

📄 Package Label / Principal Display Panel 1 words ▾

IMAGE

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

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 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 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 (69842-0349-20), 1 kit (69842-0349-30). 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.
← 69842-0347-01 · CVS 69842-0353-29 · CVS →
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.