{
  "url": "https://openlegislation.uk/prescription-only-medicines-human-use-amendment-no-2-order-2001/article-2",
  "json_url": "https://openlegislation.uk/prescription-only-medicines-human-use-amendment-no-2-order-2001/article-2.json",
  "legislation": "uksi/2001/3942",
  "legislation_title": "The Prescription Only Medicines (Human Use) Amendment (No. 2) Order 2001",
  "legislation_url": "https://openlegislation.uk/prescription-only-medicines-human-use-amendment-no-2-order-2001",
  "path": "article/2",
  "kind": "article",
  "number": "2",
  "heading": "Amendment of Schedule 1 to the principal Order",
  "text": "In Schedule 1 to the principal Order (which specifies substances which if included in medicinal products make those products prescription only medicines and exemptions from restrictions on the sale and supply of prescription only medicines)—\n(a) in relation to the substance Cetirizine Hydrochloride, the entry in column 5 is deleted;\n(b) in relation to the substance Flurbiprofen—\n(i) in column 2, there is inserted “8.75 mg”;\n(ii) in column 3, there is inserted “Throat lozenges”;\n(iii) in column 4, there is inserted “43.75 mg (MDD)”; and\n(iv) in column 5, there is inserted “Container or package containing not more than 140 mg of Flurbiprofen”;\n(c) in relation to the substance Loratadine, the entry in column 5 is deleted;\n(d) in relation to the substance Terbinafine—\n(i) in column 2, there is inserted “1.0 per cent”;\n(ii) in column 3, there is inserted “External use for the treatment of tinea pedis, tinea cruris and tinea corporis. In the form of a gel”; and\n(iii) in column 5, there is inserted “Container or package containing not more than 30 grams of medicinal product”;\n(e) there is inserted in column 1, at the appropriate place in the alphabetical order of the entries as they appear in that column, the entries set out in column 1 in the Table below, and, against those entries, there is inserted in columns 2, 3, 4 and 5 the corresponding text in columns 2, 3, 4 and 5 below:\nColumn 1\nColumn 2\nColumn 3\nColumn 4\nColumn 5\nSubstance\nMaximum strength\nRoute of administration, use, or pharmaceutical form\nTreatment limitations\nMaximum quantity\nDiphenoxylate Hydrochloride\n2.5 mg\nIn combination with Atropine Sulphate for short term use as an adjunctive therapy to appropriate rehydration in acute diarrhoea\n25 mg (MDD)\nContainer or package containing not more than 20 tablets\nFor use in persons aged 16 years and over\nTablets\nDolasetron Mesilate\nRopinirole Hydrochloride",
  "extent": null,
  "status": null,
  "version": "current",
  "annotations": [],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/uksi/2001/3942/article/2",
    "retrieved_at": "2026-10-29T07:19:22.688087+00:00"
  },
  "licence": "Open Government Licence v3.0",
  "licence_url": "https://www.nationalarchives.gov.uk/doc/open-government-licence/version/3/",
  "attribution": "Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives."
}