Crotamiton
Brand names: Eurax
Crotamiton is a topical agent used to relieve pruritus and as an adjunct in the management of scabies.
Adult dose
Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.
Contraindications
- Acute exudative dermatoses
- Hypersensitivity to the active substance or to any of the excipients
Side effects
- Pruritus (most commonly reported reaction during treatment)
- Contact dermatitis (rare)
- Hypersensitivity reactions — rash, eczema (rare)
- Erythema, skin irritation (rare)
- Angioedema (rare); discontinue treatment if severe irritation occurs
Interactions
- No interaction studies have been performed
Clinical monograph
How it works
It has antipruritic and reputed scabicidal properties, though the precise mechanism by which it relieves itch and acts on the mite is not fully established.
Prescribing in practice
- For external use only; avoid application to acutely inflamed or broken skin, near the eyes and on mucous membranes.
- It is generally regarded as a less effective scabicide than first-line treatments and is often used mainly for symptomatic itch relief.
- Itch may persist for a period after successful scabies eradication, which does not by itself indicate treatment failure.
Monitoring
Monitoring is clinical, based on relief of itching and any local skin irritation.
Counselling the patient
- Apply to intact skin and avoid contact with the eyes, mouth and broken areas.
- Itching can continue for some time after scabies has been treated and does not necessarily mean the treatment has failed.
- Stop and seek advice if a rash or marked irritation develops.
Evidence & guidelines
Crotamiton is recognised in current prescribing references as an antipruritic and adjunctive scabies treatment rather than a first-line scabicide.
Reference: Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
- Suspicious Pigmented Lesion — Melanoma Pathway · NICE NG14 2015 / BAD
- Cellulitis and Erysipelas · NICE NG141 2019 / CREST
- Psoriasis — Severity Assessment and Step-Up Therapy · NICE NG153 2019 / BAD
- Atopic Eczema — Assessment and Step-Up Therapy · NICE NG95 2023
- Urticaria and Angioedema · BSACI / EAACI Guidelines 2022
- Acne Vulgaris — Grading and Treatment · NICE NG198 2021 / BAD