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.
Note - The market status of a product is now available in the LNHPD and identifies if a product is "marketed" or "not marketed" in Canada. Product licence holders may voluntarily provide the Natural and Non-Prescription Health Products Directorate (NNHPD) with information about whether their product is currently available to Canadian consumers. Where no information has been provided, the default status is "not marketed". The "current status" field remains unaffected and will continue to indicate the status of the product licence (i.e., active, discontinued, stop sale, cancelled, or suspended). Note that where a licence has been suspended, cancelled or under stop sale, the product cannot be legally sold in Canada.
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- Natural Product Number (NPN):
- 80096808
- Market status:
- Marketed
- Licence Status:
- Active
- Brand name(s):
-
GO-LAX
;
GO-LAX BOWEL FORMULA - Licence holder:
- Healthology International Inc.
- Dosage Form:
- Capsule
- 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 | 1.0 | 2.0 | capsule | 1 | daily | |||||||
- Recommended use or purpose:
- Provides short term relief from occasional constipation For the short-term relief of occasional constipation Promotes bowel movement (by direct action on the large intestine) Supports the process of a colon cleanse by relieving occasional constipation Promotes bowel movement by direct action on the intestine Relieves occasional constipation Promotes bowel movement Laxative Cathartic
- Risk Information:
- Cautions and Warnings
- Consult a health care practitioner/health care provider/health care professional/doctor/physician prior to use if you have faecal impaction. Consult a health care practitioner prior to use if you have had recent surgery or have upcoming surgery. Keep out of reach of children Consult a health care practitioner/health care provider/health care professional/doctor/physician if symptoms persist or worsen. Consult a health care practitioner/health care provider/health care professional/doctor/ physician prior to use if you are taking cardiac medications such as cardiac glycosides or antiarrhythmic medications, thiazide diuretics, corticosteroids, licorice root or other medications or health products which may aggravate electrolyte imbalance. Consult a health care practitioner/health care provider/health care professional/doctor/ physician prior to use if you have a kidney disorder. Reduce dose or stop use if you experience abdominal pain, cramps, spasms and/or diarrhoea.
- Contra-Indications
- Do not use if you have abdominal pain of unknown origin, diarrhoea, bile duct obstruction. Do not use if you have hemorrhoids. Do not use in patients with cramps, colic, nephritis or any undiagnosed abdominal symptoms such as pain, nausea, vomiting or fever. Do not use this product if you are pregnant or breastfeeding. Do not use this product if you have abnormal constrictions of the gastrointestinal tract, potential or existing intestinal blockage, atonic bowel, appendicitis, inflammatory colon disease such as Crohn's disease or ulcerative colitis, abdominal pain of unknown origin, undiagnosed rectal bleeding, severe dehydration with depleted water or electrolytes.
- Known Adverse Reactions
- At 2 capsules per day: Some people may experience diarrhea. May cause cramp-like discomfort in the gastrointestinal tract Stop use if hypersensitivity occurs.
Medicinal ingredients | Quantity (Qty) | Extract | Potency |
---|---|---|---|
Aloe ferox |
100.0 mg
|
4.0
%
Barbaloin |
|
Magnesium |
175.0 mg
|
||
Phyllanthus emblica |
33.3 mg
|
6.006
:
1
DHE: 200 mg Dry |
|
Rheum palmatum |
100.0 mg
|
10.0
%
Rhein |
|
Terminalia bellirica |
33.3 mg
|
6.006
:
1
DHE: 200 mg Dry |
|
Terminalia chebula |
33.3 mg
|
6.006
:
1
DHE: 200 mg Dry |
|
Ulmus rubra |
50.0 mg
|
- List of non-medicinal ingredients:
-
- Gum arabic
- Hypromellose
- Oryza sativa (Rice) hull powder
- Rice bran
- Sunflower oil
- Date of licensing:
- 2020-01-24
- Revised date of licence:
- 2024-12-05
Application information
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For technical support or if you have general questions concerning the content of this database, please contact the Natural Health Products Directorate (NHPD).