Prescription medication · Topical Antiparasitic
ivermectin topical
Also sold as Soolantra. Soolantra cream treats the inflammatory bumps and pimples caused by rosacea.
Data updated 2026-05-15
- Rx
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ivermectin topical (Soolantra) is a prescription Topical Antiparasitic. Soolantra cream treats the inflammatory bumps and pimples caused by rosacea.
Soolantra cream contains ivermectin and is used on the skin. It helps treat bumps and pimples caused by rosacea.
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What it does
Soolantra cream treats the inflammatory bumps and pimples caused by rosacea.
Common side effects
Skin burning sensation, Skin irritation
Key warnings
There are no contraindications (reasons not to use) listed for this medication.
The sections below are summarized in plain English from ivermectin topical's FDA-approved prescribing information. They describe what the official label says, and are not personal medical advice.
How It Works
The exact way Soolantra works is not known. It is thought that ivermectin reduces inflammation. It may also kill certain mites that can contribute to rosacea.
Serious Warnings
There are no contraindications (reasons not to use) listed for this medication.
Common Questions
What is the active ingredient in Soolantra?
How much cream should I use?
Can I use Soolantra cream around my eyes?
How often should I apply Soolantra cream?
What should I do if I experience skin irritation?
Is Soolantra safe to use during pregnancy?
Can I use Soolantra cream on other parts of my body?
What should I do if I accidentally swallow Soolantra cream?
How long does it take to see results with Soolantra cream?
Can I use other skincare products while using Soolantra cream?
What are the common side effects of ivermectin topical?
What drug class is ivermectin topical?
What pregnancy or breastfeeding source fields are listed for ivermectin topical?
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azelaic acid
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betamethasone
Diprosone, Luxiq
Betamethasone dipropionate cream is a strong steroid medicine used on the skin.
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What the FDA Data Shows for ivermectin topical
The FDA label for ivermectin topical (sold under brand names such as Soolantra) classifies it as a prescription-only medication in the Topical Antiparasitic class. Soolantra cream treats the inflammatory bumps and pimples caused by rosacea. Official labeling lists 2 commonly reported side effects, including Skin burning sensation, Skin irritation.
Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. Voluntary reports accumulate over the lifetime of a drug and reflect wide-ranging clinical use. Interaction data is drawn directly from FDA-approved prescribing information. Acquisition-cost data is surveyed weekly by CMS and updated as manufacturers report changes.
Report counts do not establish causation, a FAERS entry documents a temporal association, not proof that the drug produced the outcome. Widely prescribed medications naturally accumulate more reports than niche therapies, so raw totals must be interpreted alongside total exposure. Shortage status, recall history, and patent information are separate source-record fields. This page is a public FDA/CMS registry and does not provide medical, treatment, substitution, or medication-change directions.
Data Sources
Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS).
FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. This registry does not provide medication decisions.
Last updated: October 24, 2024
PlainMeds is rendered directly from FDA openFDA/FAERS extracts, DailyMed labels, and CMS drug-pricing files, no number is typed in by an editor. FAERS counts, recalls, shortages, and price figures on this page are queried live from those federal extracts. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of 2026-05-15. Primary sources: openFDA / FAERS, DailyMed and CMS Part B ASP.
Read our methodology - how this data is sourced, computed, and verified.
Data currency: FDA FAERS adverse-event reports through 2025, CMS NADAC acquisition-cost pricing effective December 2024, compiled from the source snapshot dated . See our methodology for per-source dates and refresh cadence. Spot a figure that looks wrong? Report a data issue.
All federal data sources used on this page
- FDA Orange Book - approved drug products with therapeutic equivalence. accessdata.fda.gov/cder/ob
- FDA DailyMed - NIH-hosted drug labeling for FDA-approved meds. dailymed.nlm.nih.gov
- FDA Adverse Event Reporting System (FAERS) - post-marketing safety surveillance. fda.gov/drugs/faers
- NLM RxNorm - standardized clinical drug nomenclature. nlm.nih.gov/research/umls/rxnorm
- CMS Medicare Part B Drug Average Sales Price Files - federal drug pricing data. cms.gov/medicare/part-b-drugs/asp
- FDA Drug Shortages Database - current and resolved drug shortage tracking. accessdata.fda.gov/drugshortages