New Zealand - English - Medsafe (Medicines Safety Authority)

aurobindo pharma nz limited - carvedilol 12.5mg - film coated tablet - 12.5 mg - active: carvedilol 12.5mg excipient: colloidal silicon dioxide crospovidone hypromellose lactose monohydrate macrogol 400 magnesium stearate polysorbate 80 povidone purified water   sucrose titanium dioxide - indicated for the management of essential hypertension. it can be used alone or in combination with other antihypertensive agents (e.g. calcium channel blockers, diuretics).

United States - English - NLM (National Library of Medicine)

h e b - acetaminophen (unii: 362o9itl9d) (acetaminophen - unii:362o9itl9d) - acetaminophen 500 mg - pain reliever/fever reducer - temporarily relieves minor aches and pains due to: headache the common cold  backache minor pain of arthritis toothache muscular aches premenstrual and menstrual cramps - headache - the common cold  - backache - minor pain of arthritis - toothache - muscular aches - premenstrual and menstrual cramps - temporarily reduces fever

United States - English - NLM (National Library of Medicine)

the procter & gamble manufacturing company - avobenzone (unii: g63qqf2nox) (avobenzone - unii:g63qqf2nox), homosalate (unii: v06sv4m95s) (homosalate - unii:v06sv4m95s), octisalate (unii: 4x49y0596w) (octisalate - unii:4x49y0596w), octocrylene (unii: 5a68wgf6wm) (octocrylene - unii:5a68wgf6wm) - avobenzone 3 g in 100 ml

Jordan - English - JFDA (Jordan Food & Drug Administration - المؤسسة العامة للغذاء والدواء)

شركة مستودع الأدوية الأردني - the jordan drugstore co - hydrochlorothiazide 12.5 mg, valsartan 160 mg, amlodipine 10 mg - 12.5 mg, 160 mg, 10 mg

New Zealand - English - Medsafe (Medicines Safety Authority)

max health limited - dobutamine hydrochloride 14 mg/ml equivalent to dobutamine 12.5 mg/ml, 250 mg dobutamine in 20 ml;   - concentrate for infusion - 12.5 mg/ml - active: dobutamine hydrochloride 14 mg/ml equivalent to dobutamine 12.5 mg/ml, 250 mg dobutamine in 20 ml   excipient: hydrochloric acid sodium metabisulfite water for injection - dobutamine hydrochloride is indicated when inotropic support is necessary for the treatment of patients with hypoperfusion states in whom cardiac output is insufficient to meet circulatory demands. dobutamine hydrochloride is also indicated when inotropic support is required for the treatment of patients in whom abnormally increased ventricular filling pressures introduce the risk of pulmonary congestion and oedema. conditions which may precipitate such situations include the following hypoperfusion states: initially cardiac in origin: a. acute heart failure acute myocardial infarction, cardiogenic shock, following cardiac surgery, medicine-induced depression of cardiac contractility such as that which occurs in excessive ?-adrenergic receptor blockade. b. chronic heart failure acute decompensation of chronic congestive heart failure, temporary inotropic support in advanced chronic congestive heart failure, as an adjunct to therapy with conventional oral inotropic agents, systemic vasodilators, and diuretics. initially noncardiac in origin: acute hypoperfusion states secondary to trauma, surgery, sepsis, or hypovolaemia when mean arterial pressure is above 70-mm hg and pulmonary capillary wedge pressure is 18-mm hg or greater, with inadequate response to volume repletion and increased ventricular filling pressure, low cardiac output secondary to mechanical ventilation with positive end-expiratory pressure (peep). paediatric population: dobutamine is indicated in all paediatric age groups (from neonates to 18 years of age) as inotropic support in low cardiac output hypoperfusion states resulting from decompensated heart failure, following cardiac surgery, cardiomyopathies and in cardiogenic or septic shock. dobutamine stress echocardiography: dobutamine hydrochloride may be used as a substitute for physical exercise in stress testing in the diagnosis of coronary artery disease. precautions apply (refer to data sheet).

New Zealand - English - Medsafe (Medicines Safety Authority)

haleon new zealand ulc - diclofenac potassium 12.5mg;  ;  ;  ;   - liquid filled capsule - 12.5 mg - active: diclofenac potassium 12.5mg         excipient: gelatin glycerol   polysorb 85/70/00 lecithin macrogol 600 purified water quinoline yellow

United States - English - NLM (National Library of Medicine)

pronova corporation - ascorbic acid (unii: pq6ck8pd0r) (ascorbic acid - unii:pq6ck8pd0r), folic acid (unii: 935e97boy8) (folic acid - unii:935e97boy8), cyanocobalamin (unii: p6yc3eg204) (cyanocobalamin - unii:p6yc3eg204), biotin (unii: 6so6u10h04) (biotin - unii:6so6u10h04), iron (unii: e1uol152h7) (iron - unii:e1uol152h7), magnesium (unii: i38zp9992a) (magnesium - unii:i38zp9992a), zinc (unii: j41csq7qds) (zinc - unii:j41csq7qds), docusate sodium (unii: f05q2t2ja0) (docusate - unii:m7p27195ag) - ascorbic acid 100 mg - do not use maxfe for individuals with a known hypersensitivity to any of the ingredients. patients with hemochromatosis and hemosiderosis. the product is not for use in children under 12 years of age.

United States - English - NLM (National Library of Medicine)

valeant pharmaceuticals north america llc - petrolatum 46.5% - skin protectant (ointment)

United States - English - NLM (National Library of Medicine)

skinfix, inc. - allantoin 0.5% - skin protectant restores and protects lips, cuticles and dry patches.

United States - English - NLM (National Library of Medicine)

washington homeopathic products - ambra   30c - to relieve the symptoms of nervousness. indications: ambra   nervousness if symptoms persist/worsen or if pregnant/nursing, stop use and consult your practitioner.