Eurax
RxNorm 207864· CROTAMITON· TOPICAL
Journey Medical Corporation
Indications and usage
INDICATIONS AND USAGE For eradication of scabies ( Sarcoptes scabiei ) and for symptomatic treatment of pruritic skin.
Dosage and administration
DOSAGE AND ADMINISTRATION In Scabies: Thoroughly massage into the skin of the whole body from the chin down, paying particular attention to all folds and creases. A second application is advisable 24 hours later. Change clothing and bed linen the next morning. Take a cleansing bath 48 hours after the last application. In Pruritus: Massage gently into affected areas until medication is completely absorbed. Repeat as needed. DIRECTIONS FOR PATIENTS WITH SCABIES: Take a routine bath or shower. Thoroughly massage Eurax cream into the skin from the chin to the toes including folds and creases. Put Eurax cream under fingernails after trimming the fingernails short, because scabies are very likely to remain there. A toothbrush can be used to apply the Eurax cream under the fingernails. Immediately after use, wrap the toothbrush in paper and throw it away. Use of the same brush in the mouth could lead to poisoning. A second application is advisable 24 hours later. A 60 gram tube is sufficient for two applications. Change clothing and bed linen the next day. Dry clean contaminated clothing and bed linen, or wash in the hot cycle of the washing machine. Take a cleansing bath 48 hours after the last application.
Warnings
WARNINGS Discontinue treatment with this product if severe irritation or sensitization develops, and institute appropriate therapy.
Contraindications
CONTRAINDICATIONS Do not apply Eurax topically to patients who develop a sensitivity or are allergic to it or who manifest a primary irritation response to topical medications.
Drug interactions
Drug Interactions None known.
Pregnancy
Pregnancy Animal reproduction studies have not been conducted with Eurax. It is also not known whether Eurax can cause fetal harm when applied topically to a pregnant woman or can affect reproduction capacity. Eurax should be given to a pregnant woman only if clearly needed.
Adverse events
Most frequently reported events (FDA FAERS). Report frequency does not imply causation.
- pruritus61
- rash44
- pyrexia31
- malaise27
- anaemia26
- pain26
- hepatic function abnormal25
- diarrhoea21
- erythema21
- pneumonia21
- urticaria20
- rash pruritic19
- vomiting19
- constipation18
- decreased appetite18
- oedema peripheral18
Adverse reactions (label)
ADVERSE REACTIONS Primary irritation reactions, such as dermatitis, pruritus, and rash, and allergic sensitivity reactions have been reported in a few patients.
View more: Full FDA label on DailyMed →Label effective 20251217