Product information
From Health Canada
Note - The product information found within this database originates from organizations not subject to the Official Languages Act and is available in the language in which it was written and submitted to Health Canada.
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- Natural Product Number (NPN):
- 80079884
- Market status:
- Marketed
- Licence Status:
- Active
- Brand name(s):
-
M-Senna 8.6 mg
;
M-Senna - Licence holder:
- Mantra Pharma Inc.
- Dosage Form:
- Tablet
- Recommended route of administration:
-
Oral
| Sub population (Sub Pop.) | Quantity (Qty) | Frequency (Freq.) | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Sub Pop. | Age | Min. | Max. | UoM Footnote1 Age | Qty | Min. | Max. | UoM Qty | Freq. | Min. | Max. | UoM Freq. |
| Adults and Adolescents | 12 | year(s) | 2.0 | 3.0 | tablet | 1 | daily | |||||
- Recommended use or purpose:
- (Used in Herbal Medicine for the) short-term relief of occasional constipation (Used in Herbal Medicine to) promote(s) bowel movement (by direct action on the large intestine) (Traditionally used in Herbal Medicine as a) stimulant laxative.
- Risk Information:
- Cautions and Warnings
- Ask a health care professional if symptoms persist or worsen. Ask a health care professional before use if you have a kidney disorder or a lazy bowel. Ask a health care professional before use if you are taking heart medications, corticosteroids, diuretics, or other health products that may contribute to electrolyte imbalance.
- Contra-Indications
- Do not use if you are pregnant or breastfeeding. Do not use if you have inflammatory bowel disease, fever or any undiagnosed gastrointestinal trouble.
- Known Adverse Reactions
- Stop use if hypersensitivity or diarrhea occurs.
| Medicinal ingredients | Quantity (Qty) | Extract | Potency |
|---|---|---|---|
| Senna alexandrina |
43.0 milligrams
|
8
:
1
DHE: 344 milligrams Dry |
8.6
milligrams
Hydroxyanthracene derivatives |
- List of non-medicinal ingredients:
-
- Colloidal silicon dioxide
- Croscarmellose Sodium
- Magnesium Stearate
- Microcrystalline cellulose
- Polyethylene Glycol
- Polyvinyl Alcohol
- Povidone K-30
- Talc
- Date of licensing:
- 2017-09-06
- Revised date of licence:
- 2026-02-16
Application information
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