Podophyllotoxin
Brand names: Warticon, Condyline
Podophyllotoxin is a topical antimitotic agent used for external anogenital warts.
Adult dose
Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC — 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
- Open or bleeding wounds
- Concomitant use with other podophyllotoxin-containing preparations
Side effects
- Skin erosion (very common)
- Application site irritation including erythema, pruritus and skin burning sensation (very common)
- Application site hypersensitivity (post-marketing, frequency not known)
- Skin ulcer, scab, skin discolouration, blister, dry skin
- Application site pain, swelling and bleeding
Interactions
- None presently known (per SPC section 4.5)
Clinical monograph
How it works
It binds tubulin and arrests cell division in metaphase, causing necrosis of the wart tissue.
Prescribing in practice
- It is contraindicated in pregnancy because of potential toxicity, and effective contraception should be ensured in those who could become pregnant.
- Apply precisely to the wart, protecting surrounding healthy skin, and respect the limit on the area treated per application to reduce systemic absorption and local irritation.
- Treatment is given in cycles of several days followed by a rest period, repeated as directed; local irritation, erosion and soreness are common.
Monitoring
Review treated warts for response and the surrounding skin for irritation, and reassess if warts persist after the recommended cycles.
Counselling the patient
- Do not use if you are or might be pregnant.
- Apply only to the warts and protect the normal skin around them.
- Follow the treat-and-rest cycle exactly as instructed and expect some soreness.
Evidence & guidelines
Podophyllotoxin is a recognised patient-applied first-line treatment option for external anogenital warts in UK and dermatology guidance.
Reference: BASHH Anogenital Warts Guidelines 2015; NICE CKS Genital Warts; 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