Sinus Pressure and Congestion Relief Maximum Strength Pseudoephedrine HCl 30 mg Tablet, Film Coated, 24-count — NDC 11822-0112-8 (Billing 11822-0112-08)
by Rite Aid Corporation · 1 BLISTER PACK in 1 CARTON / 24 TABLET, FILM COATED in 1 BLISTER PACK
This is a package of 24 tablets of Sinus Pressure and Congestion Relief Maximum Strength Pseudoephedrine HCl 30 mg Tablet, Film Coated from Rite Aid Corporation, marketed since Aug 1981 and currently FDA-listed.
NDC 11822-0112-08
🏷️ FDA NDC (as labeled)
11822-0112-8
billing pads the package segment with a zero
This package
Contains24-count
Pack sizes2 compare ↓
🗂️ 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 →
NDC database record
One package, one record: these facts belong to NDC 11822-0112-8 alone.
- Record
- FDA NDC Directory package listing · Human OTC drug
- Code segments
- 11822 labeler · 0112 product · 8 package
- Package marketed since
- Aug 25, 1981
- Sample package
- No — commercial package
- Listing certified through
- Dec 31, 2027
- Barcode (UPC)
- 0011822319867
- FDA record last changed
- Jul 24, 2026
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
FDA NDC (as labeled)
11822-0112-8
Product NDC
11822-0112
11-digit billing NDC
11822011208
RxCUI
1049160
UNII
6V9V2RYJ8N
UPC
0011822319867
Application #
M012
SPL Set ID
d86140ab-1117-4d14-a380-f5cc375775a1
Established class (EPC)
alpha-Adrenergic Agonist
Mechanism of action
Adrenergic alpha-Agonists
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
1981-08-25
Route
ORAL
Dosage form
TABLET, FILM COATED
Substance
PSEUDOEPHEDRINE HYDROCHLORIDE
Quick answers
- RxCUI (RxNorm): 1049160
Why two NDCs?
The FDA registers this code as 11822-0112-8 — a 5-4-1 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 package segment → 11822-0112-08. 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 5, 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 alpha-Adrenergic Agonist class.
Pharmacologic class
alpha-Adrenergic Agonist
Drug family (ATC)
Sympathomimetics
How it works
Adrenergic alpha-Agonists
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
📗 Our plain-language guide HelloPharmacist
- It temporarily relieves nasal congestion from the common cold, hay fever or other upper respiratory allergies. Many products also relieve sinus congestion and pressure.
- It depends on the product. Regular tablets and softgels are usually taken every 4 to 6 hours, while 12-hour extended-release tablets are taken every 12 hours. Check your box for th...
- No. Swallow them whole. Don't divide, crush, chew or dissolve them. Seeing part of the tablet in your stool can happen and is normal.
- Can I crush or chew the extended-release tablets?
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 5, 2026
💬 Questions about Pseudoephedrine HCl?
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.
Try another pack size:
24 tablets
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 5, 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 |
|---|---|---|---|---|
| 11822-0112-02 11822-0112-2 Main listing | 2 BLISTER PACK in 1 CARTON / 24 TABLET, FILM COATED in 1 BLISTER PACK | 1981-08-25 | — | Active |
| 11822-0112-08 You're viewing this | 1 BLISTER PACK in 1 CARTON / 24 TABLET, FILM COATED in 1 BLISTER PACK | 1981-08-25 | — | Active |
Pack size FAQ
What quantity is in this package?
This is a 24-count package — 1 blister pack in 1 carton / 24 tablet, film coated in 1 blister pack.
What NDC number is used to bill for this package of Sinus Pressure and Congestion Relief Maximum Strength Pseudoephedrine HCl 30 mg Tablet, Film Coated?
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
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Good Sense Nasal Decongestant 30 mg 00113-0432-62 | L. | 24 tablets | $0.078 | — | Availability likely | — |
| Nasal Decongestant 30 mg 00536-3607-35 | Rugby | 24 tablets | $0.078 | — | Availability likely | — |
| SudoGest 30 mg 00904-5053-59 | Major | 100 tablets | $0.078 | — | Availability likely | — |
| SudoGest Nasal Decongestant 30 mg 00904-6337-24 | Major | 1 tablet | $0.078 | — | Availability likely | — |
| SudoGest 30 mg 00904-6727-60 | Major | 100 tablets | $0.078 | — | Availability likely | — |
| Pseudoephedrine HCl 30 mg 00904-6990-61 | Major | 10 tablets | $0.078 | — | Availability likely | — |
| pseudoephedrine hydrochloride 30 mg 45802-0432-62 | Padagis | 1 tablet | $0.078 | — | Availability likely | — |
| Nasal Decongestant Maximum Strength, Non-Drowsy 30 mg 46122-0428-62 | Amerisource | 24 tablets | $0.078 | — | Availability likely | — |
| Leader Nasal Decongestant 30 mg 70000-0002-01 | Cardinal | 1 tablet | $0.078 | — | Availability likely | — |
| Nasal Decongestant Maximum Strength 30 mg 70677-1017-01 | Strategic | 24 tablets | $0.078 | — | Availability likely | — |
| Nasal Decongestant D 30 mg 00363-1214-08 | Walgreen | 24 tablets | — | — | FDA listed | — |
| Sinus Pressure and Congestion Relief Maximum Strength 30 mgthis 11822-0112-08 | Rite | 24 tablets | — | — | FDA listed | — |
| Nasal Decongestant Maximum Strength 30 mg 21130-0112-08 | Better | 24 tablets | — | — | FDA listed | — |
| sinus 30 mg 30142-0613-62 | Kroger | 1 tablet | — | — | Discontinued | — |
| Sinus Decongestion 30 mg 30142-0641-08 | Kroger | 24 tablets | — | — | FDA listed | — |
| Topcare Nasal Decongestant Maximum Strength Non Drowsy 30 mg 36800-0432-62 | Topco | 1 tablet | — | — | FDA listed | — |
| Nasal Decongestant 30 mg 37808-0112-22 | H | 24 tablets | — | — | FDA listed | — |
| equaline nasal decongestant non drowsy maximum strength 30 mg 41163-0432-67 | United | 6 tablets | — | — | FDA listed | — |
| nasal decongestant maximum strength non drowsy 30 mg 41250-0432-62 | Meijer | 1 tablet | — | — | FDA listed | — |
| CareOne Nasal and Sinus Decongestant 30 mg 41520-0881-62 | American | 12 tablets | — | — | FDA listed | — |
| Sinus and Congestion Non-Drowsy 30 mg 49035-0780-08 | Wal-Mart | 24 tablets | — | — | FDA listed | — |
| Sudogest 30 mg 50090-1961-00 | A-S | 28 tablets | — | — | FDA listed | — |
| Sudogest Nasal Decongestant 30 mg 50090-4345-00 | A-S | 48 tablets | — | — | Discontinued | — |
| pseudoephedrine hydrochloride 30 mg 50090-5615-01 | A-S | 1 tablet | — | — | FDA listed | — |
| SUDAFED Sinus Congestion 30 mg 50580-0363-01 | Kenvue | 12 tablets | — | — | FDA listed | — |
| Nasal Decongestant 30 mg 50844-0112-08 | L.N.K. | 12 tablets | — | — | FDA listed | — |
| Sinus and Nasal Decongestant 30 mg 51316-0121-22 | CVS | 24 tablets | — | — | FDA listed | — |
| Sinus And Nasal Decongestant 30 mg 51316-0317-62 | CVS | 12 tablets | — | — | FDA listed | — |
| Nasal Decongestant 30 mg 56062-0432-62 | Publix | 24 tablets | — | — | FDA listed | — |
| Nasal Decongestant Non-Drowsy 30 mg 59779-0112-08 | CVS | 24 tablets | — | — | FDA listed | — |
| Nasal Decongestant 30 mg 59779-0432-62 | CVS | 1 tablet | — | — | FDA listed | — |
| Nasal Decongestant 30 mg 63187-0344-24 | Proficient | 24 tablets | — | — | FDA listed | — |
| Nasal Decongestant Maximum Strength 30 mg 63868-0802-24 | CHAIN | 24 tablets | — | — | FDA listed | — |
| Nasal Decongestant Maximum Strength 30 mg 68016-0473-24 | Chain | 24 tablets | — | — | FDA listed | — |
| pseudoephedrine hydrochloride 30 mg 71205-0197-24 | Proficient | 1 tablet | — | — | FDA listed | — |
| Sinus Congestion 30 mg 83324-0054-24 | Chain | 24 tablets | — | — | FDA listed | — |
| pseudoephedrine hydrochloride 30 mg 85766-0049-24 | Sportpharm | 1 tablet | — | — | 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 Oct 3, 2026
- CMS NADAC weekly file
Availability & generic status
🏛️
1981
On the market since
Aug 1981
📍
2026
Currently FDA-listed
45 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 Oct 3, 2026
What it looks like
Color
red
ShapeRound
Imprint44;112
Size7 mm
ScoringNot scored
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.
- FDA label on DailyMed · label index refreshed Oct 5, 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.
🧪 Avoiding an ingredient? See Pseudoephedrine inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.
Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
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 5, 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
LabelerRite Aid Corporation
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code11822
First marketedAug 1981
Product typeHuman Otc Drug
Portfolio326 products on file
More NDCs from Rite Aid Corporation labeler code 11822
- Antiseptic Mouth Rinse Eucalyptol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL Mouthwash NDC 11822-0072-1
- Athletes Foot Terbinafine Hydrochloride 1 g/100g Cream NDC 11822-0080-1
- Ibuprofen and Pseudoephedrine Hydrochloride 200 mg; 30 mg Tablet, Coated NDC 11822-0084-5
- Lanolin, Petrolatum 155 mg/g; 534 mg/g Ointment NDC 11822-0103-4
- Pain Relief Regular Strength Acetaminophen 325 mg Tablet NDC 11822-0104-1
- childrens fever reducer and pain reliever Acetaminophen 160 mg/5mL Suspension NDC 11822-0107-1
- Rite Aid Cortisone Hydrocortisone 1% 1 g/100g Spray NDC 11822-0113-3
- Antiseptic Skin Cleanser Chlorhexidine Gluconate 4% 4 g/100mL Liquid NDC 11822-0116-5
- Salicylic Acid Corn and Callus Remover Liquid .17 mg/9.8mL Liquid NDC 11822-0120-9
- Salicylic Acid Ultra Thin Corn Removers 40 mg/181 Patch NDC 11822-0123-8
- nicotine 2 mg Lozenge NDC 11822-0124-1
- Salicylic acid Medicated Callus Removers Extra Thick 40 mg/41 Patch NDC 11822-0125-4
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
📄 Do Not Use
📄 Ask a Doctor Before Use If
📄 When Using This Product
📄 Stop Use and Ask a Doctor If
🤰 If Pregnant or Breast-Feeding
📄 Keep Out of Reach of Children
📄 Questions or Comments
📄 Package Label / Principal Display Panel
🎯 Indications and Usage ▾
Uses temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies temporarily relieves sinus congestion and pressure
⏱️ Dosage and Administration ▾
Directions adults and children 12 years and over take 2 tablets every 4 to 6 hours; do not take more than 8 tablets in 24 hours children ages 6 to 11 years take 1 tablet every 4 to 6 hours; do not take more than 4 tablets in 24 hours children under 6 years do not use
⚠️ Warnings ▾
Warnings Do not use if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product. Ask a doctor before use if you have diabetes heart disease high blood pressure thyroid disease difficulty in urination due to enlargement of the prostate gland When using this product do not exceed recommended dosage.
Stop use and ask a doctor if nervousness, dizziness, or sleeplessness occur symptoms do not improve within 7 days or occur with fever If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
🧪 Active Ingredient ▾
Active ingredient (in each tablet) Pseudoephedrine HCl 30 mg
🧪 Inactive Ingredients ▾
Inactive ingredients croscarmellose sodium, dibasic calcium phosphate dihydrate, FD&C red #40 aluminum lake, FD&C yellow #6 aluminum lake, hypromellose, magnesium stearate, microcrystalline cellulose, polydextrose, polyethylene glycol, silicon dioxide, titanium dioxide, triacetin
🎯 Purpose ▾
Purpose Nasal decongestant
📄 Do Not Use ▾
Do not use if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.
📄 Ask a Doctor Before Use If ▾
Ask a doctor before use if you have diabetes heart disease high blood pressure thyroid disease difficulty in urination due to enlargement of the prostate gland
📄 When Using This Product ▾
When using this product do not exceed recommended dosage.
📄 Stop Use and Ask a Doctor If ▾
Stop use and ask a doctor if nervousness, dizziness, or sleeplessness occur symptoms do not improve within 7 days or occur with fever
🤰 If Pregnant or Breast-Feeding ▾
If pregnant or breast-feeding, ask a health professional before use.
📄 Keep Out of Reach of Children ▾
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
📄 Questions or Comments ▾
Questions or comments? 1-800-426-9391
📄 Package Label / Principal Display Panel ▾
Principal Display Panel Compare to the active ingredient in Sudafed ® Sinus Congestion* NDC 11822-0112-8 MAXIMUM STRENGTH SINUS PRESSURE & CONGESTION RELIEF PSEUDOEPHEDRINE HCl 30 mg NASAL DECONGESTANT NON-DROWSY Relieves sinus pressure, nasal and sinus congestion ACTUAL SIZE 24 TABLETS TAMPER EVIDENT: DO NOT USE IF PACKAGE IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING *This product is not manufactured or distributed by Kenvue Inc., owner of the registered trademark Sudafed® Sinus Congestion.
50844 REV0619D11208 DISTRIBUTED BY: RITE AID, 200 NEWBERRY COMMONS ETTERS, PA 17319 www.riteaid.com SATISFACTION GUARANTEE If you're not satisfied, we'll happily refund your money Rite Aid 44-112 Rite Aid 44-112
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 sinus pressure and congestion relief maximum strength (this brand).
Top reported reactions
Age at onset
Reporter sex
Male · 41%
Female · 57%
Unknown · 2%
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
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) | — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 "Otc Monograph Drug". 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 Rite Aid Corporation. 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 1 other package presentation of this same product, including 24 tablets (11822-0112-02). 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?
Rite Aid Corporation 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.