Tetraspan 6 % 60 mg/ml inf. sol. i.v. Belgija - engleski - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

tetraspan 6 % 60 mg/ml inf. sol. i.v.

b. braun melsungen ag - sodium acetate trihydrate 3,27 g/1000 ml; malic acid 0,67 mg/ml; potassium chloride 0,3 mg/ml; magnesium chloride hexahydrate 0,2 mg/ml; sodium chloride 6,25 mg/ml; hydroxyethyl starch 60 mg/ml; calcium chloride dihydrate 0,37 g/1000 ml - solution for infusion - 60 mg/ml - hydroxyethyl starch 60 mg/ml; malic acid 0.67 mg/ml; magnesium chloride hexahydrate 0.2 mg/ml; potassium chloride 0.3 mg/ml; sodium acetate trihydrate; sodium chloride 6.25 mg/ml; calcium chloride dihydrate - hydroxyethylstarch

Aripiprazole 1mg/ml Oral Solution Malta - engleski - Medicines Authority

aripiprazole 1mg/ml oral solution

brillpharma (ireland) limited inniscarra, main street, rathcoole, co. dublin, ireland - aripiprazole - oral solution - aripiprazole 1 mg/ml - psycholeptics

Calcium Plus Australija - engleski - Department of Health (Therapeutic Goods Administration)

calcium plus

procter & gamble australia pty ltd - calcium carbonate, quantity: 1.25 g (equivalent: calcium, qty 500 mg); colecalciferol, quantity: 0.005 mg - tablet, effervescent - excipient ingredients: lemon oil; maltodextrin; sucralose; sodium bicarbonate; beetroot; maize starch; citric acid; malic acid; sambucus nigra; propylene glycol; silicon dioxide; dl-alpha-tocopherol; sucrose; hydrolysed gelatin; hydrogenated soya oil; flavour - maintain/support general health and wellbeing ; maintain/support healthy teeth ; maintain/support bone health ; aids/assists healthy bone development/growth/building ; vitamin d helps calcium absorption (or words of like intent) and a diet deficient in calcium can lead to osteoporosis in later life

Baymix Latibon Plus Me Formulation:   Each kilogram contains:   Calcium Formate...... 360 g Calcium Lactate.......150 g Calcium Citrate........150 g Phosphoric Acid.......135 g Citric Acid..............60 g   Formic Acid.........50 g Lactic Acid..........43 g Sorbic Acid.........30 g Malic Acid..........45 g Feed Premix Powder Filipini - engleski - FDA (Food And Drug Administration)

baymix latibon plus me formulation: each kilogram contains: calcium formate...... 360 g calcium lactate.......150 g calcium citrate........150 g phosphoric acid.......135 g citric acid..............60 g formic acid.........50 g lactic acid..........43 g sorbic acid.........30 g malic acid..........45 g feed premix powder

elanco philippines, inc.; distributor: elanco philippines, inc. - calcium , phosphorus , organic acids (vet.) - feed premix powder - formulation: each kilogram contains: calcium formate...... 360 g calcium lactate.......150 g calcium citrate........150 g phosphoric acid.......135 g citric acid..............60 g formic acid.........50 g lactic acid..........43 g sorbic acid.........30 g malic acid..........45 g

SODIUM SULFATE, POTASSIUM SULFATE, MAGNESIUM SULFATE solution Sjedinjene Američke Države - engleski - NLM (National Library of Medicine)

sodium sulfate, potassium sulfate, magnesium sulfate solution

lupin pharmaceuticals, inc. - sodium sulfate (unii: 0ypr65r21j) (sodium sulfate anhydrous - unii:36kcs0r750), potassium sulfate (unii: 1k573lc5tv) (sulfate ion - unii:7is9n8kpmg), magnesium sulfate anhydrous (unii: ml30mj2u7i) (magnesium cation - unii:t6v3lhy838) - sodium sulfate, potassium sulfate and magnesium sulfate oral solution is indicated for cleansing of the colon as a preparation for colonoscopy in adults. - gastrointestinal obstruction - bowel perforation - gastric retention - ileus - toxic colitis or toxic megacolon - known allergies to components of the kit [see description (11)] teratogenic effects: pregnancy category c. animal reproduction studies have not been conducted with sodium sulfate, potassium sulfate and magnesium sulfate oral solution. it is also not known whether sodium sulfate, potassium sulfate and magnesium sulfate oral solution can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. sodium sulfate, potassium sulfate and magnesium sulfate oral solution should be given to a pregnant woman only if clearly needed. it is not known whether this drug is excreted in human milk. because many drugs are excreted in human milk, caution should be exercised when sodium sulfate, potassium sulfate and magnesium sulfate oral solution is administered to a nursing woman. safety and effectiveness in pediatric patients have not been established. of the 375 patients who received sodium sulfate, potassium sulfate and magnesium sulfate oral solution in clinical trials, 94 (25%) were 65 years of age or older, and 25 (7%) were 75 years of age or older. no overall differences in safety or effectiveness of sodium sulfate, potassium sulfate and magnesium sulfate oral solution administered as a split-dose (2-day) regimen were observed between geriatric patients and younger patients. geriatric patients reported more vomiting when sodium sulfate, potassium sulfate and magnesium sulfate oral solution was given as a one-day preparation.

Magnesium Strawberry Australija - engleski - Department of Health (Therapeutic Goods Administration)

magnesium strawberry

procter & gamble australia pty ltd - magnesium carbonate hydrate, quantity: 823 mg (equivalent: magnesium, qty 200 mg) - tablet, effervescent - excipient ingredients: citric acid; sodium bicarbonate; maltodextrin; lemon oil; sucralose; maize starch; malic acid; beetroot; propylene glycol; flavour - helps convert (state food) into energy ; maintain/support general health and wellbeing ; maintain/support bone health ; maintain/support muscle health ; maintain/support nervous system health

STEROFUNDIN ISO Izrael - engleski - Ministry of Health

sterofundin iso

lapidot medical import and marketing ltd - calcium chloride dihydrate; l-malic acid; magnesium chloride hexahydrate; potassium chloride; sodium acetate trihydrate; sodium chloride - solution for infusion - l-malic acid 0.67 g / 1000 ml; sodium acetate trihydrate 3.27 g / 1000 ml; calcium chloride dihydrate 0.37 g / 1000 ml; magnesium chloride hexahydrate 0.20 g / 1000 ml; potassium chloride 0.30 g / 1000 ml; sodium chloride 6.80 g / 1000 ml - electrolytes - replacement of extracellular fluid losses in the case of isotonic dehydration, where acidosis is present or imminent.

Gel-Malicid 200mg/100mg/5mL Suspension Filipini - engleski - FDA (Food And Drug Administration)

gel-malicid 200mg/100mg/5ml suspension

am-europharma corporation - aluminum hydoxide , magnesium hydroxide - suspension - 200mg/100mg/5ml

Gel-Malicid 200mg/100mg Tablet Filipini - engleski - FDA (Food And Drug Administration)

gel-malicid 200mg/100mg tablet

am-europharma corporation - aluminum hydroxide , magnesium hydroxide - tablet - 200mg/100mg

Drug Facts: Sjedinjene Američke Države - engleski - NLM (National Library of Medicine)

drug facts:

deseret biologicals, inc. - adenosine phosphate disodium (unii: t1wz11dsrn) (adenosine phosphate - unii:415shh325a), malic acid (unii: 817l1n4ckp) (malic acid - unii:817l1n4ckp), sodium diethyl oxalacetate (unii: 6ca025y4fg) (diethyl oxalacetate - unii:15s56468g7), orotic acid (unii: 61h4t033e5) (orotic acid - unii:61h4t033e5), riboflavin (unii: tlm2976ofr) (riboflavin - unii:tlm2976ofr), cinnamic acid (unii: u14a832j8d) (cinnamic acid - unii:u14a832j8d), apiole (parsley) (unii: qq67504pxo) (apiole (parsley) - unii:qq67504pxo), escher - for the temporary relief of symptoms related to common bacterial infections (respiratory and urinary tract infections, food poisoning) such as fever, headache, mucous congestion, stomach discomfort, cough, joint discomfort, and occasional diarrhea.** **these statements are based upon homeopathic principles. they have not been reviewed by the food and drug administration. for the temporary relief of symptoms related to common bacterial infections (respiratory and urinary tract infections, food poisoning) such as fever, headache, mucous congestion, stomach discomfort, cough, joint discomfort, and occasional diarrhea.** **these statements are based upon homeopathic principles. they have not been reviewed by the food and drug administration.