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Tylenol Sinus Severe Acetaminophen 325 mg; 200 mg; 5 mg Tablet, Coated — NDC 70264-0026-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Tylenol Sinus Severe Acetaminophen 325 mg; 200 mg; 5 mg Tablet, Coated — NDC 70264-026-02 (Billing 70264-0026-02)

by R J General Corporation · 50 POUCH in 1 BOX / 2 TABLET, COATED in 1 POUCH

This is a package of Tylenol Sinus Severe Acetaminophen 325 mg; 200 mg; 5 mg Tablet, Coated from R J General Corporation, marketed since May 2021 and currently FDA-listed. It is this product's only package size.

NDC 70264-0026-02
🏷️ FDA NDC (as labeled) 70264-026-02 billing pads the product segment with a zero
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 70264-026-02 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
70264 labeler · 026 product · 02 package
Package marketed since
May 1, 2021
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 7026402602 4
FDA record last changed
Jul 24, 2026
⚠️
Other active recalls for Acetaminophen (different manufacturers) — 6 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Oct 21, 2025 — Defective Container (Kenvue Brands LLC) · FDA recall D-0121-2026
Class II · Aug 20, 2025 — Discoloration (Baxter Healthcare Corporation) · FDA recall D-0596-2025
Class II · May 22, 2025 — cGMP deviations: Due to confirmed consumer complaints received with the observation of tablet discoloration (brown surface on tablets). (Aurobindo Pharma USA Inc) · FDA recall D-0471-2025
Class I · Jul 8, 2024 — Labeling: Label Mix-up: a bag of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection was found inside an overwrap labeled Acetaminophen Injection 1,000 mg per 100 mL (10 mg/mL) (Hikma Pharmaceuticals USA Inc.) · FDA recall D-0635-2024
Class II · May 20, 2024 — Discoloration: Brownish tablets (Contract Pharmacal Corporation) · FDA recall D-0566-2024
Class II · Nov 13, 2023 — Failed Impurities/Degradation Specifications (KINDER FARMS LLC) · FDA recall D-0143-2024
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 70264-026-02
Product NDC 70264-026
11-digit billing NDC 70264002602
RxCUI 1243679
UNII 362O9ITL9D, 495W7451VQ, 04JA59TNSJ
Application # M012
SPL Set ID 2cbf7954-b28f-4d7b-b142-6c6c5c58b25d
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 2021-05-01
Route ORAL
Dosage form TABLET, COATED
Substance ACETAMINOPHEN; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Quick answers
  • RxCUI (RxNorm): 1243679
Why two NDCs? The FDA registers this code as 70264-026-02 — 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 → 70264-0026-02. 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.

Clinical

📗 Our plain-language guide HelloPharmacist
  • It temporarily relieves minor aches and pains, like headache, backache, toothache, muscle aches, cold aches, minor arthritis pain and menstrual cramps. It also reduces fever.
  • Follow your product label or prescriber exactly and never exceed the maximum daily amount. Remember that the limit counts every product with acetaminophen. Too much can seriously d...
  • Check the label first. Many combination products also contain acetaminophen, and you shouldn't use two together. If you aren't sure, ask me or your pharmacist.
  • Having 3 or more alcoholic drinks every day while using it raises the risk of liver damage. If you take warfarin, talk with your doctor or pharmacist first, since regular high dail...
📖 Read our full Acetaminophen guide →
1
Nutrient depletion considerations

Acetaminophen may be associated with lower levels of 1 nutrient — worth a chat with your pharmacist, not a cause for alarm.

🧪 Full Acetaminophen nutrient depletion report →
An association is not a deficiency. Educational only — don't start or stop anything without professional guidance.
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.
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
70264-0026-02 You're viewing this Main listing 50 POUCH in 1 BOX / 2 TABLET, COATED in 1 POUCH 2021-05-01 — Active

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 — — Discontinued —
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 — — Discontinued —
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 — — Discontinued —
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 mgthis 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
May 2021
📍
2026
Currently FDA-listed
5 years listed
🔓
·
Generic versions listed
see equivalents
✅Generic appears available

FDA-approved generic versions are listed, and recent pricing/market data suggests they may be available — see Therapeutic equivalents.

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.

💡 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 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 LAV5U5022Y
    Methyl salicylate is a naturally derived liquid compound commonly found in wintergreen plants. In medicines, it's used as a flavoring agent and penetrating solvent to help distribute active ingredients evenly throughout topical products.
  • 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.

Manufacturer & labeler

LabelerR J General Corporation
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code70264
First marketedMay 2021
Product typeHuman Otc Drug
Portfolio21 products on file

More NDCs from R J General Corporation labeler code 70264

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. 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 📄 Do Not Use 📄 Ask a Doctor Before Use If 📄 Ask a Doctor or Pharmacist 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 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 49 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 21 words ▾

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

🧪 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

📄 Do Not Use 95 words ▾

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 48 words ▾

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 16 words ▾

Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin

📄 When Using This Product 9 words ▾

When using this product do not exceed recommended dose

📄 Stop Use and Ask a Doctor If 61 words ▾

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 10 words ▾

If pregnant or breast-feeding, ask a health professional before use.

📄 Keep Out of Reach of Children 6 words ▾

Keep out of reach of children.

📄 Questions or Comments 9 words ▾

Questions or comments? call 1-877-895-3665 (toll-free) or 215-273-8755 (collect)

📄 Package Label / Principal Display Panel 44 words ▾

PRINCIPAL DISPLAY PANEL TYLENOL ® FOR ADULTS SINUS SEVERE Acetaminophen, Phenylephrine HCl, Guaifenesin Pain Reliever–Fever Reducer, Nasal Decongestant, Expectorant SINUS HEADACHE SINUS PRESSURE NASAL CONGESTION MUCUS + CHEST CONGESTION DAY NON-DROWSY 50 Pouches of 2 Caplets each PRINCIPAL DISPLAY PANEL - 50 Pouch Box

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

Medicare Part D spend CMS · PART D · 2026 (Q1)

Medicare Part D (outpatient prescription) spending for Acetaminophen (matched by generic name) — the program that covers self-administered drugs. 5 manufacturers.
⚠️ Drug-level data: CMS publishes Part D spending by drug, not by NDC — these figures combine every manufacturer, strength and package size sold under the name Acetaminophen. That’s a different level of aggregation than the Medicaid card above, which is specific to this exact 11-digit NDC (pack size included), so the two aren’t directly comparable.
Period
Total Part D spend
$34K
Claims incl. refills
277
Beneficiaries
145
Spend / beneficiary
$234.25
Spend / claim
$122.62
Trend by period
💵 About the dollar figures: spending is what Part D plans paid before confidential manufacturer rebates, so the program’s real net cost is lower. A blank patient count means fewer than 11 people — CMS hides counts that small to protect privacy. Source: CMS Medicare Quarterly Part D Spending by Drug (data.cms.gov), updated quarterly.

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 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 R J General Corporation. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
R J General 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.
← 70264-0025-02 · R 70264-0027-01 · R →
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.