Home › NDC Lookup › Ingredients › Acetaminophen Guaifenesein Phenylephrine... › 42961-0112-12
Xpect Cold Relief Acetaminophen Guaifenesein Phenylephrine HCl 200 mg; 325 mg; 5 mg Tablet, 400-count — NDC 42961-0112-12 package photo

Xpect Cold Relief Acetaminophen Guaifenesein Phenylephrine HCl 200 mg; 325 mg; 5 mg Tablet, 400-count

by Cintas Corporation · 200 PACKET in 1 BOX (42961-112-12) / 2 TABLET in 1 PACKET (42961-112-10)
NDC 42961-0112-12
🏷️ FDA NDC (as labeled) 42961-112-12 billing pads the product segment with a zero
This package
Contains400-count Pack sizes4 compare ↓
Also comes in: 50 tablets 42961-0112-13 80 tablets 42961-0112-14 160 tablets 42961-0112-11
OTC Discontinued Non-controlled ⚠ Discontinued by firm
🗂️ Data synced Aug 27, 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

⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

🆔 Identity & classification

FDA NDC (as labeled) 42961-112-12
Product NDC 42961-112
11-digit billing NDC 42961011212
RxCUI 1243679
UNII 495W7451VQ, 362O9ITL9D, 04JA59TNSJ
Application # M013
SPL Set ID 02391d55-32b2-4083-9315-98e9b3650c55
Established class (EPC) Expectorant
Physiologic effect Decreased Respiratory Secretion Viscosity; Increased Respiratory Secretions
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm
Marketing start 2021-03-29
Route ORAL
Dosage form TABLET
Substance GUAIFENESIN; ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE
Why two NDCs? The FDA registers this code as 42961-112-12 — 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 → 42961-0112-12. 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 Anilides class.

Drug family (ATC) Anilides
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

LabelerCintas Corporation
FDA applicationM013 (OTC MONOGRAPH DRUG)
Labeler code42961
First marketedMar 2021
Product typeHuman Otc Drug
Portfolio30 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

📖 About the active ingredient MedlinePlus · NLM
General information about the ingredient itself — the description of this specific product follows below.

Acetaminophen is used to relieve mild to moderate pain and to reduce fever. Acetaminophen is in a class of medications called analgesics (pain relievers) and antipyretics (fever reducers). It works by changing the way the body senses pain and by cooling the body.

Read the full MedlinePlus article ↗
🧪 What is this product?

Xpect Cold Relief is an over-the-counter tablet taken by mouth that combines three active ingredients commonly used to ease cold symptoms. Acetaminophen is typically used to reduce fever and relieve pain and aches. Guaifenesin functions as an expectorant, intended to help thin mucus and make coughs more productive. Phenylephrine hydrochloride is a decongestant commonly used to help relieve nasal congestion.

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.

💊 What it looks like

Color pink
ShapeRound
Size12 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.

🧪 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.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 2S7830E561
    Crospovidone is a synthetic polymer derived from povidone. It acts as a disintegrant, helping the tablet or capsule break apart quickly in the stomach so the active ingredient can be absorbed.
  • UNII 70097M6I30
    Magnesium stearate is a salt made from magnesium and stearic acid, a fatty substance. It's used in tablets and capsules as a lubricant and glidant to help ingredients flow smoothly during manufacturing and prevent sticking.
  • UNII 7CVR7L4A2D
    A starch-derived carbohydrate produced by breaking down corn, potato, or tapioca starch. It functions as a filler and binder to give the medicine bulk and texture, and sometimes as a mild sweetener or texture enhancer in powders and tablets.
  • UNII OP1R32D61U
    Microcrystalline cellulose is a purified form of cellulose, a natural fiber from plant sources. It acts as a binder and filler in tablets and capsules, helping hold ingredients together and give the medicine its shape and size.
  • UNII 3WJQ0SDW1A
    Polyethylene glycol is a synthetic liquid or solid polymer used in medicines as a solvent, lubricant, and humectant. It helps dissolve active ingredients, reduces friction during manufacturing, and retains moisture in the final product.
  • UNII 532B59J990
    Polyvinyl alcohol is a synthetic polymer made from plant-derived materials. It's used as a binder to hold ingredients together, a film-former in coatings, and a thickener in liquid formulations.
  • UNII FZ989GH94E
    Povidone is a synthetic polymer made from a plastic-like material. It acts as a binder to hold tablet ingredients together and as a disintegrant to help the tablet break apart in your stomach so the medicine can be absorbed.
  • UNII ETJ7Z6XBU4
    Silicon dioxide is a naturally occurring mineral used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping during manufacturing and storage.
  • UNII H8AV0SQX4D
    A modified starch derived from potato or corn starch. It absorbs water quickly and helps tablets or capsules break apart and dissolve in the stomach, acting as a disintegrant to ensure the medicine releases its active ingredients properly.
  • UNII O8232NY3SJ
    A plant-based carbohydrate derived from corn kernels. It acts as a filler to add bulk, a binder to hold ingredients together, and a disintegrant to help the tablet break apart in your stomach for absorption.
  • UNII 4ELV7Z65AP
    Stearic acid is a fatty acid derived from plant or animal sources. It acts as a binder and lubricant in tablets and capsules, helping them hold together and flow smoothly during manufacturing.
  • UNII 96K6UQ3ZD4
    Sucralose is a synthetic sweetener made from sugar. It's added to medicines to improve taste without adding calories, helping make bitter or unpleasant-tasting drugs easier to take.
  • UNII 7SEV7J4R1U
    A powder made from a naturally occurring mineral. In medicines, talc works as a glidant and anti-caking agent, helping tablets and capsules flow smoothly during manufacturing and preventing clumping.
  • UNII 15FIX9V2JP
    Titanium dioxide is a bright white mineral powder commonly used as a colorant and opacifying agent. It makes pills and tablets white or lighter in color and helps make coatings non-transparent.

14 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statescorn starch, crospovidone, flavor, magnesium stearate, maltodextrin, microcrystalline cellulose, polyethylene glyvol, polyvinyl alcohol, povidone, silicone dioxide, sodium starch glycolate, stearic acid, sucralose, talc, titanium dioxide

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

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 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: 50 tablets 80 tablets 160 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Sinus Severe 325 mg/1; 200 mg/1; 5 mg 46122-0412-62 AmeriSource 12 tablets $0.111 — Availability likely —
Cold Head Congestion Severe 325 mg/1; 200 mg/1; 5 mg 46122-0415-62 AmeriSource 12 tablets $0.111 — Availability likely —
Mucus Relief Sinus Severe Congestion and Pain 325 mg/1; 200 mg/1; 5 mg 46122-0712-60 AMERISOURCE 10 tablets $0.111 — Availability likely —
Sinus Relief Severe Congestion and Pain 325 mg/1; 200 mg/1; 5 mg 70000-0080-01 CARDINAL 10 tablets $0.111 — Availability likely —
Head Congestion and Mucus 325 mg/1; 200 mg/1; 5 mg 70000-0083-01 Cardinal 12 tablets $0.111 — Availability likely —
Sinus Severe 325 mg/1; 200 mg/1; 5 mg 70677-1005-01 STRATEGIC 12 tablets $0.111 — Availability likely —
Sinus Severe 325 mg/1; 200 mg/1; 5 mg 70677-1259-01 Strategic 12 tablets $0.111 — Availability likely —
Mucus Relief Sinus Severe Congestion and Pain 325 mg/1; 200 mg/1; 5 mg 83324-0107-20 CHAIN 10 tablets $0.111 — Availability likely —
Head Congestion plus Mucus PE 325 mg/1; 200 mg/1; 5 mg 83324-0112-24 CHAIN 12 tablets $0.111 — Availability likely —
Cold plus Flu Congestion Severe 325 mg/1; 200 mg/1; 5 mg 83324-0114-24 CHAIN 12 tablets $0.111 — Availability likely —
Sinus Severe 325 mg/1; 200 mg/1; 5 mg 83324-0115-24 CHAIN 12 tablets $0.111 — Availability likely —
Mucinex Sinus-Max Severe Congestion Relief 325 mg/1; 200 mg/1; 5 mg 63824-0201-44 Reckitt 2 tablets $0.529 — FDA listed —
Severe Sinus Daytime, Non-Drowsy 325 mg/1; 200 mg/1; 5 mg 00363-5027-07 Walgreen 12 tablets — — Discontinued —
Sinus Pressure and Pain 325 mg/1; 200 mg/1; 5 mg 00363-6028-09 Walgreen 10 tablets — — FDA listed —
Severe Sinus Congestion 325 mg/1; 200 mg/1; 5 mg 00363-6150-09 Walgreen 10 tablets — — FDA listed —
Sinus Congestion and Pain Relief Non-Drowsy/Daytime 325 mg/1; 200 mg/1; 5 mg 11822-0527-08 Rite 12 tablets — — FDA listed —
severe sinus congestion relief Maximum Strength 325 mg/1; 200 mg/1; 5 mg 11822-5160-09 Rite 10 tablets — — FDA listed —
Severe Sinus Congestion and Pain Maximum Strength 325 mg/1; 200 mg/1; 5 mg 21130-0615-09 Better 10 tablets — — FDA listed —
Sinus PE Head Congestion and Mucus 325 mg/1; 200 mg/1; 5 mg 21130-0627-08 Better 12 tablets — — FDA listed —
Sinus Congestion and Pain 325 mg/1; 200 mg/1; 5 mg 30142-0727-08 Kroger 12 tablets — — FDA listed —
Daytime Sinus Severe 325 mg/1; 200 mg/1; 5 mg 30142-0732-08 Kroger 12 tablets — — FDA listed —
Sinus Relief Pressure and Pain 325 mg/1; 200 mg/1; 5 mg 30142-0828-09 Kroger 10 tablets — — FDA listed —
Sinus Congestion and Pain Severe 200 mg/1; 5 mg/1; 325 mg 36800-0505-05 TopCare 12 tablets — — FDA listed —
Cold and Head Congestion Severe 325 mg/1; 200 mg/1; 5 mg 36800-0575-02 TopCo 12 tablets — — FDA listed —
Head Congestion plus Mucus PE 325 mg/1; 200 mg/1; 5 mg 36800-0793-02 TOPCARE 12 tablets — — FDA listed —
Head Congestion plus Mucus PE 325 mg/1; 200 mg/1; 5 mg 37808-0273-02 HEB 12 tablets — — FDA listed —
Mucus Relief Sinus Severe Congestion Relief 325 mg/1; 200 mg/1; 5 mg 37808-0367-02 HEB 10 tablets — — FDA listed —
Cold Head Congestion Severe 325 mg/1; 200 mg/1; 5 mg 37808-0775-02 HEB 12 tablets — — FDA listed —
Head Congestion Plus Mucus PE 325 mg/1; 200 mg/1; 5 mg 41163-0712-02 United 12 tablets — — FDA listed —
sinus severe 325 mg/1; 200 mg/1; 5 mg 41250-0219-05 Meijer 12 tablets — — FDA listed —
mucus relief sinus severe congestion and pain 325 mg/1; 200 mg/1; 5 mg 41250-0267-02 Meijer 10 tablets — — Discontinued —
Cold Relief Severe Head Congestion 325 mg/1; 200 mg/1; 5 mg 41250-0275-02 Meijer 12 tablets — — FDA listed —
head congestion plus mucus PE 325 mg/1; 200 mg/1; 5 mg 41250-0573-02 MEIJER 12 tablets — — Discontinued —
Head Congestion plus Mucus PE 325 mg/1; 200 mg/1; 5 mg 42507-0173-02 HYVEE 12 tablets — — FDA listed —
Sinus Severe 325 mg/1; 200 mg/1; 5 mg 42507-0219-05 HYVEE 12 tablets — — FDA listed —
Cold plus Head Congestion Severe 325 mg/1; 200 mg/1; 5 mg 42507-0375-02 HYVEE 12 tablets — — FDA listed —
Xpect Cold Relief 200 mg/1; 325 mg/1; 5 mgthis 42961-0112-12 Cintas 400 tablets — — Discontinued —
Severe Congestion Relief Maximum Strength Sinus 325 mg/1; 200 mg/1; 5 mg 49035-0165-09 Wal-Mart 10 tablets — — FDA listed —
Sinus Congestion and Pain Severe 325 mg/1; 200 mg/1; 5 mg 49035-0527-08 Wal-Mart 12 tablets — — FDA listed —
Tylenol Sinus Severe 325 mg/1; 200 mg/1; 5 mg 50269-0507-25 JC 2 tablets — — FDA listed —
Tylenol Sinus Severe 325 mg/1; 200 mg/1; 5 mg 50269-0551-01 JC 2 tablets — — FDA listed —
SUDAFED PE Head Congestion Plus Mucus 325 mg/1; 200 mg/1; 5 mg 50580-0447-01 Kenvue 12 tablets — — FDA listed —
Tylenol Sinus Severe 325 mg/1; 200 mg/1; 5 mg 50580-0507-01 Kenvue 12 tablets — — FDA listed —
Tylenol Cold Plus Head Congestion Severe 325 mg/1; 200 mg/1; 5 mg 50580-0566-25 Kenvue 12 tablets — — FDA listed —
Head Congestion Mucus PE 325 mg/1; 200 mg/1; 5 mg 50804-0173-02 GOODSENSE 12 tablets — — FDA listed —
Sinus Severe 325 mg/1; 200 mg/1; 5 mg 50804-0672-05 GoodSense 12 tablets — — FDA listed —
Cold and Head Congestion Severe 325 mg/1; 200 mg/1; 5 mg 50804-0805-03 GoodSense 12 tablets — — FDA listed —
Sinus Severe 325 mg/1; 200 mg/1; 5 mg 50844-0572-02 L.N.K. 12 tablets — — FDA listed —
Mucus Relief Sinus Severe Congestion and Pain 325 mg/1; 200 mg/1; 5 mg 51316-0516-09 CVS 10 tablets — — FDA listed —
Severe Sinus Pain and Congestion 325 mg/1; 200 mg/1; 5 mg 51316-0927-08 CVS 12 tablets — — FDA listed —
Tylenol Sinus Severe 325 mg/1; 200 mg/1; 5 mg 53209-1004-02 Morning 2 tablets — — FDA listed —
Mucus Relief Sinus Severe Congestion Relief 325 mg/1; 200 mg/1; 5 mg 53943-0167-02 DISCOUNT 10 tablets — — FDA listed —
Cold Plus Head Congestion Severe 325 mg/1; 200 mg/1; 5 mg 53943-0175-02 DISCOUNT 12 tablets — — FDA listed —
Sinus Severe 325 mg/1; 200 mg/1; 5 mg 53943-0319-05 DISCOUNT 12 tablets — — FDA listed —
Severe Congestion and Pain 325 mg/1; 200 mg/1; 5 mg 55319-0815-19 Family 8 tablets — — FDA listed —
Sinus Severe Daytime 325 mg/1; 200 mg/1; 5 mg 55910-0529-08 DOLGENCORP, 12 tablets — — FDA listed —
Cold and Head Congestion Severe 325 mg/1; 200 mg/1; 5 mg 55910-0927-08 DOLGENCORP, 12 tablets — — FDA listed —
Severe Sinus Pain and Congestion Daytime 325 mg/1; 200 mg/1; 5 mg 59779-0275-08 CVS 12 tablets — — FDA listed —
Maximum Strength Mucinex Sinus-Max Severe Congestion and Pain 325 mg/1; 200 mg/1; 5 mg 63824-0241-10 Reckitt 10 tablets — — FDA listed —
Mucinex Sinus-Max Severe Congestion and Pain, Maximum Strength 325 mg/1; 200 mg/1; 5 mg 63824-0243-20 Reckitt 10 tablets — — FDA listed —
Severe Sinus Congestion and Pain 325 mg/1; 200 mg/1; 5 mg 63868-0071-24 Chain 12 tablets — — FDA listed —
Severe Cold Head Congestion 325 mg/1; 200 mg/1; 5 mg 63868-0081-24 Chain 12 tablets — — FDA listed —
Head Congestion Mucus PE 325 mg/1; 200 mg/1; 5 mg 63868-0103-24 CHAIN 12 tablets — — FDA listed —
Mucus Relief Sinus Severe Congestion Relief 325 mg/1; 200 mg/1; 5 mg 63868-0722-20 Chain 10 tablets — — FDA listed —
Pressure Pain Mucus PE 325 mg/1; 200 mg/1; 5 mg 63868-0747-24 Chain 12 tablets — — FDA listed —
Mucus Relief Sinus Severe Congestion Relief 325 mg/1; 200 mg/1; 5 mg 63941-0167-02 VALU 10 tablets — — FDA listed —
Pressure and Pain Plus Mucus PE 325 mg/1; 200 mg/1; 5 mg 63941-0173-02 VALU 12 tablets — — FDA listed —
Sinus Severe 325 mg/1; 200 mg/1; 5 mg 63941-0275-08 Valu 12 tablets — — FDA listed —
Non-Drowsy Sinus Severe, Circle K 325 mg/1; 200 mg/1; 5 mg 66715-5544-09 Lil' 2 tablets — — FDA listed —
Non-Drowsy Sinus Severe, Circle K 200 mg/1; 5 mg/1; 325 mg 66715-5632-03 Lil' 2 tablets — — FDA listed —
Sinus Relief, Caseys 4good 325 mg/1; 200 mg/1; 5 mg 66715-6332-03 Lil' 6 tablets — — FDA listed —
Tylenol Sinus Severe, Lil Drug Store 325 mg/1; 200 mg/1; 5 mg 66715-6457-07 Lil 2 tablets — — FDA listed —
Tylenol Sinus Severe, CVP HEALTH 325 mg/1; 200 mg/1; 5 mg 66715-6557-02 Lil 2 tablets — — FDA listed —
Daytime Sinus Severe 200 mg/1; 5 mg/1; 325 mg 66715-6744-09 Lil' 2 tablets — — FDA listed —
Tylenol Sinus Severe, TRAVEL BASIX 325 mg/1; 200 mg/1; 5 mg 66715-7857-02 Lil 2 tablets — — FDA listed —
Lil Drug Store Tylenol Sinus Severe 325 mg/1; 200 mg/1; 5 mg 66715-9757-02 Lil 2 tablets — — FDA listed —
Cold and Head Congestion Relief Severe 325 mg/1; 200 mg/1; 5 mg 67091-0212-24 WinCo 12 tablets — — FDA listed —
Nasal Decongestant PE and Pain Relief Plus Mucus Relief 325 mg/1; 200 mg/1; 5 mg 67091-0349-24 Winco 12 tablets — — FDA listed —
Tylenol Sinus Severe 325 mg/1; 200 mg/1; 5 mg 67414-0507-00 Jones 2 tablets — — FDA listed —
Tylenol Sinus Severe 325 mg/1; 200 mg/1; 5 mg 67751-0239-01 Navajo 2 tablets — — FDA listed —
Sinus Severe 325 mg/1; 200 mg/1; 5 mg 68016-0504-24 CHAIN 12 tablets — — Discontinued —
Mucus Relief Sinus Severe Congestion Relief 325 mg/1; 200 mg/1; 5 mg 68016-0549-20 CHAIN 10 tablets — — Discontinued —
Cold and Head Congestion Severe 325 mg/1; 200 mg/1; 5 mg 68016-0717-24 CHAIN 12 tablets — — Discontinued —
Severe Cold Head Congestion 325 mg/1; 200 mg/1; 5 mg 68998-0175-02 Marc 12 tablets — — FDA listed —
Sinus Severe 325 mg/1; 200 mg/1; 5 mg 68998-0219-05 MARC 12 tablets — — FDA listed —
Cold plus Head Congestion Severe 325 mg/1; 200 mg/1; 5 mg 68998-0275-02 MARC 12 tablets — — FDA listed —
Congestion and Headache 325 mg/1; 200 mg/1; 5 mg 69842-0651-01 CVS 10 tablets — — FDA listed —
Mucus Relief Sinus Severe Congestion and Pain 325 mg/1; 200 mg/1; 5 mg 69842-0786-02 CVS 10 tablets — — Discontinued —
Tylenol Sinus Severe 325 mg/1; 200 mg/1; 5 mg 70264-0026-02 R 2 tablets — — FDA listed —
Sinus Severe 325 mg/1; 200 mg/1; 5 mg 72036-0119-05 Harris 12 tablets — — FDA listed —
Mucus Relief Sinus Severe Congestion and Pain 325 mg/1; 200 mg/1; 5 mg 72036-0167-02 HARRIS 10 tablets — — FDA listed —
Cold Head Congestion Severe 325 mg/1; 200 mg/1; 5 mg 72036-0175-02 Harris 12 tablets — — FDA listed —
Sinus Sevre 325 mg/1; 200 mg/1; 5 mg 72476-0119-05 RETAIL 12 tablets — — FDA listed —
Severe Congestion and Pain 325 mg/1; 200 mg/1; 5 mg 72476-0167-02 Retail 10 tablets — — FDA listed —
Tylenol Sinus Severe 325 mg/1; 200 mg/1; 5 mg 73097-0014-02 Savings 2 tablets — — FDA listed —
Cold and Head Congestion Severe 325 mg/1; 200 mg/1; 5 mg 79481-3572-08 Meijer 12 tablets — — FDA listed —
Pressure, Pain and Mucus 325 mg/1; 200 mg/1; 5 mg 79481-5072-08 Meijer 12 tablets — — FDA listed —
Severe Congestion and Pain 325 mg/1; 200 mg/1; 5 mg 79481-5196-09 Meijer 10 tablets — — FDA listed —
Sinus Severe Non Drowsy, Daytime 325 mg/1; 200 mg/1; 5 mg 79481-7250-08 Meijer 12 tablets — — FDA listed —
Severe Sinus Congestion and Pain 325 mg/1; 200 mg/1; 5 mg 83059-0029-01 Shield 12 tablets — — Discontinued —
Severe Sinus Congestion and Pain 325 mg/1; 200 mg/1; 5 mg 83059-0057-01 Shield 12 tablets — — FDA listed —
Severe Sinus Congestion and Pain 325 mg/1; 200 mg/1; 5 mg 83059-0107-01 Shield 12 tablets — — FDA listed —
Severe Sinus Congestion and Pain 325 mg/1; 200 mg/1; 5 mg 83059-0121-06 Shield 60 tablets — — 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

🏛️
2021
On the market since
Mar 2021
📍
2026
Currently FDA-listed
5 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 NDCDescription Marketing startStatus
42961-0112-11 80 PACKET in 1 BOX (42961-112-11) / 2 TABLET in 1 PACKET (42961-112-10) 2021-03-29 Discontinued by firm
42961-0112-12 You're viewing this 200 PACKET in 1 BOX (42961-112-12) / 2 TABLET in 1 PACKET (42961-112-10) 2022-12-30 Discontinued by firm
42961-0112-13 25 PACKET in 1 BAG (42961-112-13) / 2 TABLET in 1 PACKET (42961-112-10) 2025-09-23 Active
42961-0112-14 40 PACKET in 1 BOX (42961-112-14) / 2 TABLET in 1 PACKET (42961-112-10) 2025-09-23 Active

Pack size FAQ

What quantity is in NDC 42961-0112-12?
NDC 42961-0112-12 is a 400-count package — 200 packet in 1 box / 2 tablet in 1 packet.
What is the difference between NDC 42961-0112-12 and NDC 42961-0112-13?
Both are Xpect Cold Relief Acetaminophen Guaifenesein Phenylephrine HCl 200 mg; 325 mg; 5 mg Tablet — the drug itself is identical. NDC 42961-0112-12 is the 400-count package, while NDC 42961-0112-13 is the 50 tablets package.
What NDC number is used to bill for this package of Xpect Cold Relief Acetaminophen Guaifenesein Phenylephrine HCl 200 mg; 325 mg; 5 mg Tablet?
Bill NDC 42961-0112-12 — the 11-digit billing format is 42961011212. 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 No longer marketed (per FDA listing data)
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 "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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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 42961-112-12, 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: 42961-0112-12, written without dashes as 42961011212. 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 42961-0112-12, the first segment (42961) is the labeler code FDA assigned to Cintas Corporation; the middle segment (0112) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (12) identifies this exact package size and type. Together they name one specific package of one specific product.
Does this product come in other package sizes?
Yes — the FDA directory lists 3 other package presentations of this same product, including 50 tablets (42961-0112-13), 80 tablets (42961-0112-14), 160 tablets (42961-0112-11). 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?
Cintas 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.

📄 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 44 words ▾

Uses temporarily relieves these symptoms associated with hay fever or other respiratory allergies, and the common cold: headache, nasal congestion, minor aches and pains, sinus congestion and pressure helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive temporarily reduces fever

⏱️ Dosage and Administration 46 words ▾

Directions do not take more than directed adults and children 12 years and over: take 2 caplets every 4 hours; swallow whole - do not crush, chew, or dissolve; do not take more than 10 caplets in 24 hours children under 12 years: ask a doctor

⚠️ Warnings 68 words ▾

Warnings Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take more than 4,000 mg of acetaminophen in 24 hours with other drugs containing acetaminophen 3 or more alcoholic drinks every day while using this product Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include: blisters, rash, skin reddening. If a skin reaction occurs, stop use and seek medical help right away.

🧪 Active Ingredient 15 words ▾

Active ingredients (in each caplet) Acetaminophen 325 mg Guaifenesin 200 mg Phenylephrine HCl 5 mg

🧪 Inactive Ingredients 27 words ▾

Inactive ingredients corn starch, crospovidone, flavor, magnesium stearate, maltodextrin, microcrystalline cellulose, polyethylene glyvol, polyvinyl alcohol, povidone, silicone dioxide, sodium starch glycolate, stearic acid, sucralose, talc, titanium dioxide

🎯 Purpose 7 words ▾

Purpose Pain reliever/fever reducer Expectorant Nasal decongestant

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 42961-0109-02 · Cintas 42961-0120-02 · Cintas →
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.