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Tylenol Sinus Severe Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride 325 mg; 200 mg; 5 mg Tablet, Coated — NDC 67751-0239-02 package photo

Tylenol Sinus Severe Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride 325 mg; 200 mg; 5 mg Tablet, Coated

by Navajo Manufacturing Company Inc. · 2 POUCH in 1 CARTON (67751-239-02) / 2 TABLET, COATED in 1 POUCH
NDC 67751-0239-02
🏷️ FDA NDC (as labeled) 67751-239-02 billing pads the product segment with a zero
This package
Contains2 tablet, coated in 1 pouch Pack sizes2 compare ↓
Also comes in: 2 tablets 67751-0239-01
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 →

This page is curated, coded, and maintained by

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

🆔 Identity & classification

FDA NDC (as labeled) 67751-239-02
Product NDC 67751-239
11-digit billing NDC 67751023902
RxCUI 1243679
UNII 362O9ITL9D, 495W7451VQ, 04JA59TNSJ
Application # M012
SPL Set ID 435b4a2a-d6bf-ec25-e063-6294a90a3f06
Established class (EPC) Expectorant
Physiologic effect Decreased Respiratory Secretion Viscosity; Increased Respiratory Secretions
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-02-19
Route ORAL
Dosage form TABLET, COATED
Substance ACETAMINOPHEN; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Why two NDCs? The FDA registers this code as 67751-239-02 — 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 → 67751-0239-02. 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

LabelerNavajo Manufacturing Company Inc.
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code67751
First marketedFeb 2025
Product typeHuman Otc Drug
Portfolio60 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?

Tylenol Sinus Severe is an oral tablet containing three active ingredients commonly used together for sinus and cold symptoms. Acetaminophen is typically used to reduce fever and ease pain or achiness. Guaifenesin functions as an expectorant, commonly included in products to help thin mucus. Phenylephrine hydrochloride is a decongestant typically used to help relieve nasal congestion. This product is an over-the-counter monograph drug, meaning it is marketed under FDA's established rules for this category of combination cold and sinus products.

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 white
ShapeOval
ImprintTYLENOL;1072
Size2 mm
ScoringNot scored
FlavorMint
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 R12CBM0EIZ
    A natural wax derived from a Brazilian palm tree, used as a coating and polish on tablets and capsules. It creates a smooth, shiny finish that protects the medicine and improves appearance.
  • UNII M28OL1HH48
    Croscarmellose sodium is a plant-based substance derived from cellulose. It acts as a disintegrant, helping tablets and capsules break down quickly in the digestive system so the medicine can be absorbed.
  • UNII 9XZ8H6N6OH
    A plant-based cellulose derivative used as a binder to hold tablet ingredients together, a thickener in liquids, and a coating agent to control how fast the medicine dissolves.
  • UNII 3NXW29V3WO
    Hypromellose is a plant-based thickener made from cellulose. It's used in medicines as a binder to hold ingredients together, a coating for tablets, and a thickener for liquids.
  • 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 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 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 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.
  • UNII XHX3C3X673
    Triacetin is a clear, oily liquid made from glycerin and acetic acid. It works as a plasticizer and solvent in medicines, helping soften coatings and improve how liquids mix together in formulations.

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

The official label also statescarnauba wax, croscarmellose sodium, flavor, hydroxypropyl cellulose, hypromellose, magnesium stearate, microcrystalline cellulose, pregelatinized starch, sucralose, titanium dioxide, triacetin

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: 2 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 $0.105 — Availability likely —
Cold Head Congestion Severe 325 mg/1; 200 mg/1; 5 mg 46122-0415-62 AmeriSource 12 tablets $0.105 — Availability likely —
Mucus Relief Sinus Severe Congestion and Pain 325 mg/1; 200 mg/1; 5 mg 46122-0712-60 AMERISOURCE 10 tablets $0.105 — Availability likely —
Sinus Relief Severe Congestion and Pain 325 mg/1; 200 mg/1; 5 mg 70000-0080-01 CARDINAL 10 tablets $0.105 — Availability likely —
Head Congestion and Mucus 325 mg/1; 200 mg/1; 5 mg 70000-0083-01 Cardinal 12 tablets $0.105 — Availability likely —
Sinus Severe 325 mg/1; 200 mg/1; 5 mg 70677-1005-01 STRATEGIC 12 tablets $0.105 — Availability likely —
Sinus Severe 325 mg/1; 200 mg/1; 5 mg 70677-1259-01 Strategic 12 tablets $0.105 — Availability likely —
Mucus Relief Sinus Severe Congestion and Pain 325 mg/1; 200 mg/1; 5 mg 83324-0107-20 CHAIN 10 tablets $0.105 — Availability likely —
Head Congestion plus Mucus PE 325 mg/1; 200 mg/1; 5 mg 83324-0112-24 CHAIN 12 tablets $0.105 — Availability likely —
Cold plus Flu Congestion Severe 325 mg/1; 200 mg/1; 5 mg 83324-0114-24 CHAIN 12 tablets $0.105 — Availability likely —
Sinus Severe 325 mg/1; 200 mg/1; 5 mg 83324-0115-24 CHAIN 12 tablets $0.105 — 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 mg 42961-0112-11 Cintas 160 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 mgthis 67751-0239-02 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 —
Tylenol Sinus Severe 325 mg/1; 200 mg/1; 5 mg 85237-1955-01 Select 2 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

🏛️
2025
On the market since
Feb 2025
📍
2026
Currently FDA-listed
1 year 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.

🔬 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 Tylenol Sinus Severe (this brand).

Top reported reactions

Hypertension3
Nasopharyngitis3
Nausea3
Vomiting3
Covid-192
Decreased Appetite2
Diarrhoea2

Age at onset

Adult3
Elderly5

Reporter sex

33 reports
Male · 27%
Female · 73%

Serious outcomes

Hospitalization2
Reports over time (by year) — tap or hover for the count & year
2022 2023 2024 2026 7 3
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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
67751-0239-01 1 POUCH in 1 CARTON (67751-239-01) / 2 TABLET, COATED in 1 POUCH 2025-02-19 Active
67751-0239-02 You're viewing this 2 POUCH in 1 CARTON (67751-239-02) / 2 TABLET, COATED in 1 POUCH 2025-02-19 Active

Pack size FAQ

What quantity is in NDC 67751-0239-02?
NDC 67751-0239-02 is listed by the FDA — 2 pouch in 1 carton / 2 tablet, coated in 1 pouch.
What NDC number is used to bill for this package of Tylenol Sinus Severe Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride 325 mg; 200 mg; 5 mg Tablet, Coated?
Bill NDC 67751-0239-02 — the 11-digit billing format is 67751023902. 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
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.
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 67751-239-02, 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: 67751-0239-02, written without dashes as 67751023902. 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 67751-0239-02, the first segment (67751) is the labeler code FDA assigned to Navajo Manufacturing Company Inc.; the middle segment (0239) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) 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 Navajo Manufacturing Company 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 1 other package presentation of this same product, including 2 tablets (67751-0239-01). 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?
Navajo Manufacturing Company 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 📦 Storage and Handling 🧪 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: sinus congestion and pressure headache nasal congestion minor aches and pains helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive temporarily reduces fever

⏱️ Dosage and Administration 48 words ▾

Directions do not take more than directed (see overdose warning) 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 ~2 min read ▾

Warnings Liver warning This product contains acetaminophen. The maximum daily dose of this product is 10 caplets (3,250 mg acetaminophen) in 24 hours. 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: skin reddening blisters rash If a skin reaction occurs, stop use and seek medical help right away. Do not use with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist. 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. if you have ever had an allergic reaction to this product or any of its ingredients. Ask a doctor before use if you have liver disease heart disease high blood pressure thyroid disease diabetes trouble urinating due to an enlarged prostate gland persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema cough that occurs with too much phlegm (mucus) Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin When using this product do not exceed recommended dose Stop use and ask a doctor if nervousness, dizziness, or sleeplessness occur pain, nasal congestion or cough gets worse or lasts more than 7 days fever gets worse or lasts more than 3 days redness or swelling is present new symptoms occur cough comes back or occurs with rash or headache that lasts These could be signs of a serious condition.

If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. Overdose warning In case of overdose, get medical help or contact a Poison Control Center right away.

(1-800-222-1222) Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

📦 Storage and Handling 22 words ▾

Other information each caplet contains: sodium 3 mg store between 20-25°C (68-77°F) do not use if blister unit is torn or broken

🧪 Active Ingredient 22 words ▾

Active ingredients (in each caplet) Purpose Acetaminophen 325 mg Pain reliever/fever reducer Guaifenesin 200 mg Expectorant Phenylephrine HCl 5 mg Nasal decongestant

🧪 Inactive Ingredients 20 words ▾

Inactive ingredients carnauba wax, croscarmellose sodium, flavor, hydroxypropyl cellulose, hypromellose, magnesium stearate, microcrystalline cellulose, pregelatinized starch, sucralose, titanium dioxide, triacetin

🎯 Purpose 22 words ▾

Active ingredients (in each caplet) Purpose Acetaminophen 325 mg Pain reliever/fever reducer Guaifenesin 200 mg Expectorant Phenylephrine HCl 5 mg Nasal decongestant

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 67751-0238-15 · Navajo 67751-0240-01 · Navajo →
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.