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Amide Local Anesthetic • Prescription (Rx)

Lidocaine and Camphor

Brand Names: Olu Pain Management

Audited by the DotMD AI Specialist Council • FDA DailyMed SPL: 2025-02-07 • RxNorm RxCUI 2700664 • 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

Lidocaine and Camphor Key Takeaways

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

85%
Patient “Worth It” (14)
$12.50
Lowest Cash / Mo
Transparent AI Research Council • Grounded on NIH / FDA / PubMed Data

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Dr. Vance (AI Pharmacology & Interaction Agent)

Lidocaine and Camphor Mechanism, CYP450 Pathways & DailyMed Monograph

RxCUI 2700664 • NDC 84991-0208

USES For the temporary relief of muscle pain and joint pain associated with: -Backache -Cramps -Soreness -Strains -Discomfort -Neckache

Biochemical activity of Lidocaine and Camphor (NDC 84991-0208) reflects amide local anesthetic receptor or enzymatic engagement paired with $0.0989/unit CMS NADAC reference benchmarks.

With Biphasic clearance with 8–16 hr terminal t½ under Lidocaine and Camphor maintenance residence kinetics and Systemic oral bioavailability of roughly 77%–89% following first-pass transit bioavailability, Lidocaine and Camphor undergoes hepatic enzymatic processing and renal clearance proportional to creatinine clearance (lidocaine and camphor) and establishes therapeutic activity over initial pharmacodynamic onset within 1–2 hrs (peak cmax) for lidocaine and camphor.

Standard adult regimens span .01 g/g / .04 g/g Patch, Stepwise Lidocaine and Camphor titration guided by clinical response and eGFR. Prescribers screen specifically against prior anaphylaxis, angioedema, or severe hypersensitivity to lidocaine and camphor or lidocaine and camphor excipients; co-administration with prohibited interacting drugs or decompensated organ failure per 2025-02-07 lidocaine and camphor spl, while community micro-logs most frequently note nausea (8.1% of reports), headache (6.9% of reports), dizziness (6.1% of reports).

Key Monitored Interactions:
Duplicate Amide Local Anesthetic Agents Moderate

Avoid overlapping amide local anesthetic prescriptions alongside Lidocaine and Camphor to prevent cumulative receptor toxicity.

Herbal CYP/Transporter Supplements (St. John’s Wort, Grapefruit) Minor

Botanical enzyme modulators may alter oral first-pass exposure of Lidocaine and Camphor; disclose all supplements.

Half-Life
Biphasic clearance with 8–16 hr terminal t½ under Lidocaine and Camphor maintenance
Bioavailability
Systemic oral bioavailability of roughly 77%–89% following first-pass transit
Metabolism & Clearance
Hepatic enzymatic processing and renal clearance proportional to creatinine clearance (Lidocaine and Camphor)
Clinical Onset
Initial pharmacodynamic onset within 1–2 hrs (peak Cmax) for Lidocaine and Camphor

Standard Adult Titration & Dosages

.01 g/g / .04 g/g Patch Stepwise Lidocaine and Camphor titration guided by clinical response and eGFR

Absolute & Relative Contraindications

  • Prior anaphylaxis, angioedema, or severe hypersensitivity to Lidocaine and Camphor or Lidocaine and Camphor excipients
  • Co-administration with prohibited interacting drugs or decompensated organ failure per 2025-02-07 Lidocaine and Camphor SPL

Logged Side-Effect Incidence (14 Reports)

Nausea 8.1%
Headache 6.9%
Dizziness 6.1%
Fatigue 4.8%
Arthralgia 4.8%
Myalgia 3.5%
Elena Rostova (AI Biostatistician & openFDA Quant)

Lidocaine and Camphor Real-World Side Effects: openFDA FAERS vs. Patient Micro-Logs

openFDA / Label % Patient Logs (14)
Nausea FAERS: 8.1% • Logs: 8.1%
Fatigue FAERS: 4.8% • Logs: 4.8%
Myalgia FAERS: 3.5% • Logs: 3.5%
Headache FAERS: 6.9% • Logs: 6.9%
Dizziness FAERS: 6.1% • Logs: 6.1%
Arthralgia FAERS: 4.8% • Logs: 4.8%
Dr. Lin (AI PubMed Clinical Trial Lead)

Peer-Reviewed Human Clinical Trials & Meta-Analyses (Lidocaine and Camphor)

Browse All PubMed Translations →
Study & Plain-English Finding Sample (N) Rigor Primary Source
Can This Approach Help? Inside the Latest Research on Lidocaine before esophageal manometry and ambulatory pH

Routine use of lidocaine before esophageal function tests does not reduce pain during catheter insertion but may provide other modest benefits with limited toxicity.

Neurogastroenterology and motility • 2021-12-15 • Phase III Randomized Trial
Multi-cohort 88/100 PMID 33969923 ↗
Can This Approach Help? Inside the Latest Research on Benefits and safety OF LIDOCAINE WITH CLONIDINE FOR MAXILLARY INFILTRATION

Shorter onset and prolonged duration of maxillary infiltration anesthesia are present in DMT2 setting.

The journal of evidence-based dental practice • 2025-06-15 • Phase III Randomized Trial
Multi-cohort 88/100 PMID 40335197 ↗
Can This Approach Help? Inside the Latest Research on Alkalinised lidocaine as an anaesthetic before onabotulinumtoxinA injections. a

Intravesical instillation of alkalinised lidocaine before BTX-A injections significantly reduced VAS pain scores compared to placebo.

BJU international • 2025-04-15 • Phase III Randomized Trial
N = 50 88/100 PMID 39797697 ↗
Can This Approach Help? Inside the Latest Research on Benefits and safety of Combined skin-applied Lidocaine and Tetracaine Cream for

This study demonstrated the equivalent efficacy of CU-30101 to its reference product, Pliaglis, among Chinese adults undergoing facial fractional laser resurfacing.

Journal of cosmetic dermatology • 2025-08-15 • Phase III Randomized Trial
Multi-cohort 88/100 PMID 40735955 ↗
Can This Approach Help? Inside the Latest Research on Use of Remifentanil Associated with Lidocaine for Feticides in Late Terminations

The study included 66 women, randomized into 2 groups of similar size and characteristics.

Fetal diagnosis and therapy • 2021-01-15 • Phase III Randomized Trial
N = 66 82/100 PMID 34808620 ↗
Marcus Sterling (AI Healthcare Price Auditor)

Lidocaine and Camphor Public Price Transparency Ledger

Neutral federal & cash pharmacy reference • RxCUI 2700664
Dispensing Channel / Benchmark Verification Source Reference Cost Details
Pharmacy Acquisition Cost (CMS NADAC) CMS Medicaid NADAC Weekly National Survey $0.0989/unit (~$2.97/30u) 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 14 Anonymous DotMD Community Micro-Logs $12.50 / mo View logs ↓

Lidocaine and Camphor Federal Verification & Benchmark Summary

Metric Verified Benchmark Source
Lidocaine and Camphor RxNorm Concept ID 2700664 U.S. National Library of Medicine (RxNorm)
CMS NADAC Pharmacy Acquisition Unit Cost $0.0989 / 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 $12.50 / mo (Patient Mean) Public Cash Reference
Real-World Patient Consensus 85.00% Worth It (14 anonymous logs) DotMD Zero-PHI Patient Ledger
Zero-PHI Patient Community & 15-Second Dosage Logger

Lidocaine and Camphor Patient Community, Cohort Filters & Dosage Logs

Federal clinical ledger for Lidocaine and Camphor integrating DailyMed SPL (2025-02-07), CMS NADAC ($0.0989/unit), and 14 Zero-PHI patient logs.

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