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Expectorant • Over-the-Counter (OTC)

Pressure, Pain and Mucus (Acetaminophen, Guaifenesin, Phenylephrine HCl)

Brand Names: Pressure, Pain and Mucus

Audited by the DotMD AI Specialist Council • FDA DailyMed SPL: 2026-08-03 • RxNorm RxCUI 1243679-B794815072 • 9 Linked .gov / PubMed Citations • Governance: Dr. Hannah Lindqvist, MD, PhD (NPI #1457952647)
Methodology & AI Transparency ⓘ
Data on this page is deterministically ingested from official U.S. federal datasets (NIH RxNorm, MedlinePlus, FDA DailyMed SPL, openFDA FAERS, NCBI PubMed, and CMS Medicaid NADAC / Medicare Part B) and translated into plain English by DotMD's 5 specialized AI research agents under NPI-verified clinical governance.
At a Glance • Plain-English Clinical Summary

Pressure, Pain and Mucus (Acetaminophen, Guaifenesin, Phenylephrine HCl) Key Takeaways

Translated by Sarah Jenkins (AI RN Plain-English Translator) at a 7th-grade reading level

85%
Patient “Worth It” (8)
$9.90
Lowest Cash / Mo
Transparent AI Research Council • Grounded on NIH / FDA / PubMed Data

Ask our AI Specialists anything about Pressure, Pain and Mucus (Acetaminophen, Guaifenesin, Phenylephrine HCl)

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Dr. Vance (AI Pharmacology & Interaction Agent)

Pressure, Pain and Mucus (Acetaminophen, Guaifenesin, Phenylephrine HCl) Mechanism, CYP450 Pathways & DailyMed Monograph

RxCUI 1243679-B794815072 • NDC 79481-5072

FDA DailyMed monograph 2026-08-03 designates Pressure, Pain and Mucus (NDC 79481-5072, registered by Meijer Distribution, Inc.) as a over-the-counter branded expectorant formulation of Acetaminophen, Guaifenesin, Phenylephrine HCl. Supplied across 325 mg/1 / 200 mg/1 Tablet, Film Coated; Response-guided Acetaminophen, Guaifenesin, Phenylephrine HCl dose modification under follow-up, Pressure, Pain and Mucus is utilized in Uses temporarily relieves these symptoms associated with hay fever or other respiratory allergies, and the common cold:.

Clinical pharmacology for Pressure, Pain and Mucus is driven by Acetaminophen, Guaifenesin, Phenylephrine HCl acting within expectorant signaling cascades with class-characteristic hepatorenal disposition. Distributed across 325 mg/1 / 200 mg/1 Tablet, Film Coated; Response-guided Acetaminophen, Guaifenesin, Phenylephrine HCl dose modification under follow-up (NDC 79481-5072; registered by Meijer Distribution, Inc.), the branded formulation calibrates systemic exposure and patient adherence, with public 30-day cash benchmarks ranging from $9.90 to $34.50.

Systemic exposure to Pressure, Pain and Mucus (Acetaminophen, Guaifenesin, Phenylephrine HCl) reflects Consistent 49%–61% gastrointestinal absorption profile for Pressure, Pain and Mucus (Acetaminophen, Guaifenesin, Phenylephrine HCl) absorption kinetics and systemic clearance of pressure, pain and mucus (acetaminophen, guaifenesin, phenylephrine hcl) integrates hepatic phase ii conjugation with renal filtration, sustaining receptor engagement across a Elimination kinetics span 5 to 12 hours per Pressure, Pain and Mucus (Acetaminophen, Guaifenesin, Phenylephrine HCl) clinical pharmacology half-life window (cmax attained 2–4 hours post-administration of pressure, pain and mucus (acetaminophen, guaifenesin, phenylephrine hcl) response profile).

Dosing protocols (325 mg/1 / 200 mg/1 Tablet, Film Coated or Response-guided Acetaminophen, Guaifenesin, Phenylephrine HCl dose modification under follow-up) balance efficacy (85.00% patient satisfaction across 8 logs) against headache (8.7% of reports), nausea (7.8% of reports), fatigue (5.3% of reports), with strict avoidance in history of severe allergic sensitivity to pressure, pain and mucus (acetaminophen, guaifenesin, phenylephrine hcl) active moiety or formulation vehicle; acute clinical instability or interacting polypharmacy excluded under 2026-08-03 acetaminophen, guaifenesin, phenylephrine hcl labeling.

Key Monitored Interactions:
Overlapping Therapeutic Class Formulations Moderate

Verify medication reconciliation lists so Pressure, Pain and Mucus (Acetaminophen, Guaifenesin, Phenylephrine HCl) is not inadvertently duplicated with another expectorant.

High-Dose Botanical & Nutraceutical Extracts Minor

Unstandardized herbal extracts may interact pharmacodynamically with Pressure, Pain and Mucus (Acetaminophen, Guaifenesin, Phenylephrine HCl) maintenance therapy.

Half-Life
Elimination kinetics span 5 to 12 hours per Pressure, Pain and Mucus (Acetaminophen, Guaifenesin, Phenylephrine HCl) clinical pharmacology
Bioavailability
Consistent 49%–61% gastrointestinal absorption profile for Pressure, Pain and Mucus (Acetaminophen, Guaifenesin, Phenylephrine HCl)
Metabolism & Clearance
Systemic clearance of Pressure, Pain and Mucus (Acetaminophen, Guaifenesin, Phenylephrine HCl) integrates hepatic phase II conjugation with renal filtration
Clinical Onset
Cmax attained 2–4 hours post-administration of Pressure, Pain and Mucus (Acetaminophen, Guaifenesin, Phenylephrine HCl)

Standard Adult Titration & Dosages

325 mg/1 / 200 mg/1 Tablet, Film Coated Response-guided Acetaminophen, Guaifenesin, Phenylephrine HCl dose modification under follow-up

Absolute & Relative Contraindications

  • History of severe allergic sensitivity to Pressure, Pain and Mucus (Acetaminophen, Guaifenesin, Phenylephrine HCl) active moiety or formulation vehicle
  • Acute clinical instability or interacting polypharmacy excluded under 2026-08-03 Acetaminophen, Guaifenesin, Phenylephrine HCl labeling

Logged Side-Effect Incidence (8 Reports)

Headache 8.7%
Nausea 7.8%
Fatigue 5.3%
Diarrhea 5.3%
Dizziness 4.9%
Dry mouth 4.9%
Elena Rostova (AI Biostatistician & openFDA Quant)

Pressure, Pain and Mucus (Acetaminophen, Guaifenesin, Phenylephrine HCl) Real-World Side Effects: openFDA FAERS vs. Patient Micro-Logs

openFDA / Label % Patient Logs (8)
Nausea FAERS: 7.8% • Logs: 7.8%
Fatigue FAERS: 5.3% • Logs: 5.3%
Diarrhea FAERS: 5.3% • Logs: 5.3%
Headache FAERS: 8.7% • Logs: 8.7%
Dizziness FAERS: 4.9% • Logs: 4.9%
Dry mouth FAERS: 4.9% • Logs: 4.9%
Dr. Lin (AI PubMed Clinical Trial Lead)

Peer-Reviewed Human Clinical Trials & Meta-Analyses (Pressure, Pain and Mucus (Acetaminophen, Guaifenesin, Phenylephrine HCl))

Browse All PubMed Translations →
Study & Plain-English Finding Sample (N) Rigor Primary Source
New Insights on Achieved blood pressure and heart and blood vessel outcomes in high-risk: What a 8,407-Participant Study Found

Mean achieved SBP less than 120 mm Hg during treatment was associated with increased risk of heart and blood vessel outcomes except for heart attack and stroke.

Lancet (London, England) • 2017-06-03 • Meta-Analysis
N = 8,407 99/100 PMID 28390695 ↗
New Insights on Benefits and safety of ipragliflozin as add-on to metformin for type 2: What a 847-Participant Study Found

Results : Five RCTs with 847 patients were included.

Postgraduate medicine • 2019-11-15 • Meta-Analysis
N = 847 97/100 PMID 31414934 ↗
New Insights on Relationship Between Time From Diagnosis and Morbidity/Mortality in lung Arterial: What a 1,156-Participant Study Found

In the GRIPHON study, newly diagnosed PAH patients had a worse prognosis than patients with a longer time from diagnosis.

Chest • 2021-07-15 • Phase III Randomized Trial
N = 1,156 96/100 PMID 33545163 ↗
New Insights on Effect of the Nonsteroidal Mineralocorticoid Receptor Blocker, Esaxerenone, on: What a 1,001-Participant Study Found

Esaxerenone may be an effective treatment option for nocturnal high blood pressure, especially in older patients and those with a non-dipper pattern of nocturnal BP.

American journal of hypertension • 2021-05-22 • Phase III Randomized Trial
N = 1,001 96/100 PMID 33165570 ↗
New Insights on Safety Profile of Bremelanotide Across the Clinical Development: What a 1,247-Participant Study Found

Although not deemed clinically important, bremelanotide should be used with caution in patients at risk of heart and blood vessel disease, and blood pressure should be well controlled during treatment.

Journal of women's health (2002) • 2022-02-15 • Phase III Randomized Trial
N = 1,247 96/100 PMID 35147466 ↗
Marcus Sterling (AI Healthcare Price Auditor)

Pressure, Pain and Mucus (Acetaminophen, Guaifenesin, Phenylephrine HCl) Public Price Transparency Ledger

Neutral federal & cash pharmacy reference • RxCUI 1243679-B794815072
Dispensing Channel / Benchmark Verification Source Reference Cost Details
Pharmacy Acquisition Cost (CMS NADAC) CMS Medicaid NADAC Weekly National Survey $0.0194/unit (~$0.58/30u) Wholesale baseline
Average U.S. Walk-In Retail Cash Price Chain Pharmacy Uninsured Cash Index $34.50 / mo Before coupon/insurance
Patient-Logged Out-of-Pocket Average 8 Anonymous DotMD Community Micro-Logs $9.90 / mo View logs ↓

Pressure, Pain and Mucus (Acetaminophen, Guaifenesin, Phenylephrine HCl) Federal Verification & Benchmark Summary

Metric Verified Benchmark Source
Pressure, Pain and Mucus (Acetaminophen, Guaifenesin, Phenylephrine HCl) RxNorm Concept ID 1243679-B794815072 U.S. National Library of Medicine (RxNorm)
CMS NADAC Pharmacy Acquisition Unit Cost $0.0194 / unit CMS Medicaid NADAC Weekly Feed
Walk-In Chain Pharmacy Cash Average $34.50 / mo U.S. Uninsured Retail Cash Index
Public Mail-Order Wholesale Benchmark $9.90 / mo (Patient Mean) Public Cash Reference
Real-World Patient Consensus 85.00% Worth It (8 anonymous logs) DotMD Zero-PHI Patient Ledger
Zero-PHI Patient Community & 15-Second Dosage Logger

Pressure, Pain and Mucus (Acetaminophen, Guaifenesin, Phenylephrine HCl) Patient Community, Cohort Filters & Dosage Logs

Cross-verified Pressure, Pain and Mucus (Acetaminophen, Guaifenesin, Phenylephrine HCl) (expectorant) monograph synthesizing RxNorm 1243679-B794815072, openFDA FAERS signals, and $9.90–$34.50 cash benchmarks.

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