Skip to content
ClinCalc Pro
Menu
Potent topical corticosteroid Pregnancy: No or limited data in pregnant women and insufficient animal reproductive toxicity data for hydrocortisone 17-butyrate; more potent corticosteroids have been teratogenic in animals after dermal application, so use during pregnancy only when the potential benefit justifies the potential risk. Breastfeeding: can be used, as systemic absorption after topical application is low, but avoid applying directly on the breast

Hydrocortisone butyrate

Brand names: Locoid

Used in: Anaphylaxis & Allergy

Hydrocortisone butyrate is a potent topical corticosteroid used for steroid-responsive inflammatory skin conditions such as eczema and dermatitis.

Auto-extracted from the source labelling — not yet independently clinician-verified. These values were distilled from the UK SPC (or the US label where noted) but have not had a clinician sign-off. Confirm against the current SmPC before prescribing.

Adult dose

Dose: Apply a thin and even layer to the affected area of skin
Route: Cutaneous (topical cream)
Frequency: 1 to 2 times daily
Source: eMC SPC for Locoid Cream (hydrocortisone butyrate), §4.2. The same dose is used for adults and older people — clinical evidence indicates no special dosage regimen is necessary in older people. Application may be made under occlusion in the more resistant lesions such as thickened psoriatic plaques on elbows and knees, but occlusion should be restricted to dermatoses involving limited areas. PAEDIATRIC: no numeric or per-kg paediatric dose is stated. The SPC states that in the paediatric population long-term treatment, large amounts and occlusion should be avoided, and that in infants therapy should be limited to a maximum of seven days. Verify paediatric use against a children's formulary. Do not apply to the eyelids (risk of glaucoma simplex or subcapsular cataract) and keep away from the eyes. Avoid application to the face, genitals, flexures and other areas of thin skin (skin atrophy and increased absorption). Wash hands after each application unless treating the hands. Increased risk of systemic and local adverse reactions when treating intertriginous areas or large areas of skin, under occlusion, with frequent dosing, or with long treatment periods — including adrenocortical suppression. Contraindicated on infected skin; use with particular caution at sites of previous or suspected infection. Topical steroid withdrawal syndrome may follow long-term use — suspect if the condition recurs within days to weeks of successful treatment. Refer to an ophthalmologist if blurred vision or other visual disturbance occurs. Fire risk: instruct patients not to smoke or go near naked flames. The bundle also contains a US label for Hydrocortisone Butyrate Lotion 0.1% (apply a thin layer twice daily for up to 2 weeks; reassess if no improvement at 2 weeks; weigh benefit against risk before extending to 4 weeks; avoid occlusion and the diaper area; US paediatric use established from 3 months of age) — a different formulation, not used for this 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

  • Hypersensitivity to the active substance or to any of the excipients
  • Untreated viral, fungal, yeast or parasitic infections
  • Tubercular or syphilitic lesions
  • Peri-oral dermatitis, acne vulgaris and rosacea
  • Bacterial infections, unless used in connection with appropriate chemotherapy

Side effects

  • Hypersensitivity (rare); skin irritation reported in clinical studies
  • Skin atrophy (often irreversible, with thinning of the epidermis), telangiectasia, skin striae, purpura
  • Dermatitis and eczema, including contact dermatitis; erythema, pruritus, rash; acne, perioral dermatitis, skin depigmentation
  • Adrenal suppression (endocrine)
  • Blurred vision
  • Withdrawal reactions and rebound effect — redness of the skin which may extend beyond the initial affected area, burning or stinging sensation, itch, skin peeling, oozing pustules; application site pain

Clinical monograph

How it works

It binds glucocorticoid receptors in skin cells to produce anti-inflammatory, immunosuppressive and vasoconstrictive effects; despite the hydrocortisone name, the butyrate ester confers potent activity.

Prescribing in practice

  • Note that, unlike plain hydrocortisone, hydrocortisone butyrate is a potent steroid, so apply the lowest effective amount for the shortest time and take particular care on the face and flexures to limit atrophy and systemic absorption.
  • Reserve for inflammatory dermatoses requiring a potent agent and step down as control is achieved.
  • Do not apply to untreated bacterial, fungal or viral skin infection.

Monitoring

No routine laboratory monitoring is required; review for treatment response and local corticosteroid adverse effects such as skin thinning.

Counselling the patient

  • This is a strong steroid despite its name; apply thinly to affected areas only and not as a general moisturiser.
  • Avoid the face and skin folds unless specifically directed and do not use on infected skin.
  • Continue regular emollients alongside treatment.

Evidence & guidelines

Topical corticosteroids are central to NICE eczema management, with potent agents such as hydrocortisone butyrate selected by disease severity and site.

Reference: NICE CG57; 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.