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Topical Antibiotic/Antiprotozoal — Rosacea Pregnancy: US label: Pregnancy Category B. There has been no experience to date with the use of metronidazole 0.75% topical gel in pregnant patients. Metronidazole crosses the placental barrier and enters the fetal circulation rapidly; because oral metronidazole has been shown to be a carcinogen in some rodents, this drug should be used during pregnancy only if clearly needed. (UK oral SPC: there is inadequate evidence of safety in pregnancy; should not be given during pregnancy or lactation unless the physician considers it essential.)

Metronidazole Topical

Brand names: Rozex, Metrogel, Metrosa

Used in: Sepsis Acute Appendicitis

Topical metronidazole is an antimicrobial and anti-inflammatory preparation applied to the face for the inflammatory papules and pustules of rosacea.

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 and rub in a thin film of metronidazole 0.75% topical gel to the entire affected area twice daily, morning and evening, after washing
Route: Topical (cutaneous)
Frequency: Twice daily (morning and evening)
SOURCE / ROUTE FLAG: the UK SPC fetched into this bundle is Metronidazole 200 mg Film-Coated TABLETS (oral route, systemic anaerobic/protozoal infections) — that posology does NOT apply to this topical monograph and has deliberately not been used. The dose above is taken verbatim from the US label for metronidazole 0.75% topical gel; the UK SPC for the topical product (gel/cream) still needs to be sourced and the strength, frequency and licensed indication (e.g. rosacea) verified. Areas to be treated should be cleansed before application; patients may use cosmetics after application. Paediatric: safety and effectiveness of the topical gel in paediatric patients have not been established; no per-kg dose is stated.

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

  • History of hypersensitivity to metronidazole, to parabens, or to other ingredients of the formulation
  • (Oral metronidazole SPC, for reference only) known hypersensitivity to nitroimidazoles, metronidazole or any excipient

Side effects

  • Burning at the application site
  • Skin irritation and dryness
  • Transient redness
  • Metallic taste
  • Tingling or numbness of extremities; nausea

Interactions

  • Oral metronidazole has been reported to potentiate the anticoagulant effect of coumarin and warfarin, prolonging prothrombin time; the effect of topical metronidazole on prothrombin time is not known

Clinical monograph

How it works

In rosacea its benefit is attributed mainly to anti-inflammatory and antioxidant effects on the skin rather than to a classical antibacterial mechanism.

Prescribing in practice

  • For external use only; avoid contact with the eyes and apply only to affected areas of the face.
  • Advise avoidance of excessive sunlight, as some patients report photosensitivity.
  • Apply a thin film to the affected skin once or twice daily as directed, and expect a gradual response over weeks.

Monitoring

Monitoring is clinical, assessing improvement in inflammatory rosacea lesions and any local irritation or dryness.

Counselling the patient

  • Apply a thin layer to the affected areas as directed and keep it away from the eyes.
  • Improvement is gradual, so continue the treatment course even if results are slow.
  • Avoid known rosacea triggers and protect your face from strong sun.

Evidence & guidelines

Topical metronidazole is an established first-line option for papulopustular rosacea and is recommended within NICE clinical guidance.

Reference: BAD Rosacea Guidelines 2017; ATTRACT Trial (Taieb et al. Br J Dermatol 2015); NICE CKS Rosacea; 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.