{"id":562937,"title":"Non-prescription Drugs: Labelling Standards - Drug Product - Canada.ca","sourceCode":"hc","sourceName":"Health Canada","language":"en","captureDate":"2026-02-16","captureTimestamp":"2026-02-16T10:31:15.495000+00:00","jobId":6,"originalUrl":"https://www.canada.ca/en/health-canada/services/drugs-health-products/drug-products/applications-submissions/guidance-documents/nonprescription-drugs-labelling-standards.html","snippet":"Non-prescription Drugs: Labelling Standards - Drug Product A non-prescription drug labelling standard outlines the permissible conditions of use and labelling requirements, such as dose, intended use, directions for use, warnings, active ingredients and combinations thereof.…","rawSnapshotUrl":"/api/snapshots/raw/562937","browseUrl":"https://replay.healtharchive.ca/job-6/20260216103115/https://www.canada.ca/en/health-canada/services/drugs-health-products/drug-products/applications-submissions/guidance-documents/nonprescription-drugs-labelling-standards.html#ha_snapshot=562937","mimeType":"text/html","statusCode":200,"captureBackend":"browsertrix","captureFidelity":"high"}