Canada · Health Canada Drug Product Database
IBUPROFEN DAYTIME, IBUPROFEN NIGHTTIME
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 92126
- DIN
- 02436949
- Form
- Capsule, Kit
- Company as listed by source
- VITA HEALTH PRODUCTS INC
- Source status
- Approved (2015-02-16)
- Source last updated
- 2026-06-23
Source-listed ingredients
- IBUPROFEN (IBUPROFEN, IBUPROFEN POTASSIUM) — 200 MG
- IBUPROFEN (IBUPROFEN POTASSIUM, IBUPROFEN) — 200 MG
- DIPHENHYDRAMINE HYDROCHLORIDE — 25 MG
These values do not establish equivalence or a dose recommendation.
Packages
- Daytime 12/24 - Nighttime 6/12
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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