Glucox
Country: Australia
Language: English
Source: Department of Health (Therapeutic Goods Administration)
Public Assessment Report
(PAR)
29-09-2019
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Active ingredient:
bovine sodium chondroitin sulfate, Quantity: 273.92 mg (Equivalent: chondroitin sulfate, Qty 250 mg); glucosamine hydrochloride, Quantity: 500 mg; hydrolysed collagen, Quantity: 200 mg; dimethyl sulfone, Quantity: 100 mg
Available from:
Vitex Pharmaceuticals Pty Ltd
Pharmaceutical form:
Capsule, hard
Composition:
Excipient Ingredients: colloidal anhydrous silica; magnesium stearate; Gelatin; purified water
Administration route:
Oral
Therapeutic indications:
Maintain/support general health and wellbeing ; Maintain/support joint health
Product summary:
Visual Identification: ;
Authorization status:
Listed
Authorization date:
2019-08-29
