IMODIUM MULTI-SYMPTOM RELIEF
LOE Approachingloperamide hydrochloride and dimethicone
NDAORALTABLET
Approved
Nov 2000
Lifecycle
LOE Approaching
Competitive Pressure
30/100
Data completeness
2/8 — Basic
Drug data last refreshed 6d ago · AI intelligence enriched 2w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
IMODIUM MULTI-SYMPTOM RELIEF is an oral tablet combining loperamide hydrochloride (an antidiarrheal agent) and dimethicone (an anti-gas agent) to address both diarrhea and associated gastrointestinal discomfort. The combination targets multiple symptoms of acute gastroenteritis and functional diarrhea in a single formulation. This is an OTC product designed for symptomatic relief rather than disease modification.
LOE Approaching
As an OTC product approaching loss of exclusivity with moderate competitive pressure (30% intensity), the brand team is likely consolidating around line extensions, cost management, and retail channel optimization rather than expansion.
Mechanism of Action
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Career Relevance
Working on IMODIUM MULTI-SYMPTOM RELIEF offers experience in OTC portfolio management, retail channel dynamics, and competitive defense in a mature market, but limited upside in terms of career growth or innovation exposure. This is a consolidation and optimization role rather than a launch or growth opportunity; professionals should expect to build skills in cost management, generic mitigation, and operational efficiency.
Brand Manager (OTC)
Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.