Chlorhexidine with nystatin
Brand names: Nystaform
A topical/cutaneous preparation combining chlorhexidine, a cationic biguanide antiseptic, with nystatin, a polyene antifungal, used to treat or prevent superficial bacterial and candidal skin infection, particularly in moist or macerated flexural areas.
Adult dose
Dose independently re-sourced from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — clinician-reviewed. Always confirm against the product SmPC and your local formulary before prescribing.
Contraindications
- Known hypersensitivity to the active substance, especially in those with a history of possible chlorhexidine-related allergic reactions, or to any of the excipients
Side effects
- Allergic skin reactions such as dermatitis, pruritus, erythema, eczema, rash, urticaria, skin irritation and blisters (frequency not known)
- Hypersensitivity, including anaphylactic shock (frequency not known) - chlorhexidine is known to induce generalised allergic reactions
- Local skin reactions (e.g. contact dermatitis) attributed to cetostearyl alcohol
- Allergic reactions and mild local irritation attributed to benzyl alcohol (10 mg per gram of cream)
Interactions
- None stated in the SPC (section 4.5: 'None stated.')
Clinical monograph
How it works
Chlorhexidine disrupts bacterial cell membranes and is bactericidal against a broad range of organisms, while nystatin binds ergosterol in the fungal cell membrane, increasing permeability and killing Candida species.
Prescribing in practice
- Nystatin is not absorbed through intact skin and chlorhexidine has negligible systemic absorption, so the principal risk is local irritation or contact sensitisation rather than systemic toxicity.
- Keep chlorhexidine away from the eyes, middle ear and meninges, as it can cause irritation of these tissues.
- Reserve for confirmed or strongly suspected mixed bacterial and candidal infection rather than routine use, to limit sensitisation and resistance.
Monitoring
No laboratory monitoring is required; review the treated area clinically and stop if irritation, worsening or no improvement occurs.
Counselling the patient
- Apply a thin layer to the affected area as directed and keep the skin clean and as dry as possible.
- Stop and seek advice if the skin becomes more red, itchy or sore, which may indicate a reaction.
Evidence & guidelines
Topical antiseptic-antifungal combinations are long-established for superficial mixed skin infection; choice should follow local guidance and infection-control principles.
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