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
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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.
How to Take It
Apply Soolantra cream to the affected areas of your face once a day. Use a pea-sized amount for each area, like your forehead, chin, nose, and each cheek. Spread the cream as a thin layer, but avoid your eyes and lips.
This is a plain-language summary of ivermectin topical's FDA labeling, not individualized dosing advice. Ask a pharmacist or prescriber before changing how you take this medication.
Pregnancy & Breastfeeding
It is not known if Soolantra cream can harm an unborn baby. Talk to your doctor if you are pregnant or plan to become pregnant. It is also not known if Soolantra passes into breast milk.
This is a plain-language summary of ivermectin topical's FDA labeling, not individualized advice. Ask a pharmacist or prescriber about pregnancy or breastfeeding on this medication.
Missed Dose
If you miss a dose, apply it as soon as you remember. Then, continue with your regular schedule.
This is a plain-language summary of ivermectin topical's FDA labeling, not individualized advice. Ask a pharmacist or prescriber what to do about your specific missed dose.
Storage
Store Soolantra cream at room temperature, between 68°F and 77°F.
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?
Is ivermectin topical safe during pregnancy?
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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 further shape supply and switching decisions. This page summarizes public FDA data for educational purposes only and is not a substitute for professional medical advice, always consult a licensed healthcare provider before starting, stopping, or changing any medication.
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. Always consult a healthcare professional before making medication decisions.
Last updated: October 24, 2024
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 and last refreshed May 2026. See our methodology for per-source dates and refresh cadence. Spot a figure that looks wrong? Report a correction.
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