Hydrodol After Powder

Country: Australia

Language: English

Source: Department of Health (Therapeutic Goods Administration)

Active ingredient:

glucose monohydrate, Quantity: 270 mg/g; pyridoxine hydrochloride, Quantity: 0.414 mg/g (Equivalent: pyridoxine, Qty 0.34 mg/g); ascorbic acid, Quantity: 9 mg/g; sodium citrate dihydrate, Quantity: 58 mg/g; sodium chloride, Quantity: 51.99 mg/g (Equivalent: sodium, Qty 20.46 mg/g); cyanocobalamin, Quantity: 0.48 microgram/g; nicotinamide, Quantity: 2.93 mg/g; calcium pantothenate, Quantity: 1.2 mg/g (Equivalent: pantothenic acid, Qty 1.1 mg/g); riboflavin, Quantity: 0.48 mg/g; Zingiber officinale, Quantity: 10 mg/g (Equivalent: Zingiber officinale, Qty 200 mg/g); citric acid, Quantity: 124 mg/g; sodium bicarbonate, Quantity: 46 mg/g; thiamine hydrochloride, Quantity: 2.8 mg/g; d-alpha-tocopheryl acetate, Quantity: 1.783 mg/g (Equivalent: d-alpha-tocopheryl acetate, Qty 0.918 mg/g); potassium chloride, Quantity: 30 mg/g (Equivalent: potassium, Qty 15.73 mg/g); calcified lithothamnion tophiforme, Quantity: 61.05 mg/g; betacarotene, Quantity: 0.296 mg/g; Curcuma longa, Quantity: 15 mg/g (Equivalent: Curcuma longa, Qty 300 mg/g; Equivalent: curcuminoids (of Curcuma longa), Qty 6.69 mg/g)

Available from:

Substance Pty Ltd

Pharmaceutical form:

Powder, oral

Composition:

Excipient Ingredients: colloidal anhydrous silica; inulin; Stevia rebaudiana; maltodextrin; modified food starch; malic acid; citric acid monohydrate; purified water; Acacia; sodium alginate; Pea Starch; betadex; Flavour

Administration route:

Oral

Therapeutic indications:

Maintain/support energy production ; Maintain/support body electrolyte balance ; Maintain/support general health and wellbeing ; Traditionally used in Western herbal medicine to Maintain/support healthy digestion ; Traditionally used in Western herbal medicine to Decrease/reduce/relieve symptoms of motion/travel/sea sickness

Product summary:

Visual Identification: ; Container Type: Sachet; Container Closure: Neither child resistant closure nor restricted flow insert

Authorization status:

Listed

Authorization date:

2020-07-23