COMFAROL FORTE paracetamol 500 mg and codeine phosphate hemihydrate 30 mg tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

comfarol forte paracetamol 500 mg and codeine phosphate hemihydrate 30 mg tablet blister pack

sanofi-aventis australia pty ltd - codeine phosphate hemihydrate, quantity: 30 mg; paracetamol, quantity: 500 mg - tablet, uncoated - excipient ingredients: povidone; pregelatinised maize starch; croscarmellose sodium; maize starch; potassium sorbate; microcrystalline cellulose; stearic acid; magnesium stearate; purified talc - comfarol forte is indicated for the short-term management of severe pain for which other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain.

Comfarol Forte Australia - English - Department of Health (Therapeutic Goods Administration)

comfarol forte

sanofi-aventis australia pty ltd - paracetamol; codeine phosphate -

Combizar 50 mg/12.5 mg Tablet Philippines - English - FDA (Food And Drug Administration)

combizar 50 mg/12.5 mg tablet

unilab, inc.; distributor: n/a - losartan potassium , hydrochlorothiazide - tablet - 50 mg/12.5 mg

COMBIZAR 100mg / 25mg Tablet Philippines - English - FDA (Food And Drug Administration)

combizar 100mg / 25mg tablet

unilab, inc.; distributor: united laboratories, inc. - losartan potassium , hydrochlorothiazide - tablet - 100mg / 25mg

Combizar 50mg/12.5mg Film-Coated Tablet Philippines - English - FDA (Food And Drug Administration)

combizar 50mg/12.5mg film-coated tablet

sandoz philippines corporation; distributor: unilab, inc. - losartan potassium , hydrochlorothiazide - film-coated tablet - 50mg/12.5mg

Combizar 100mg/25mg Film-Coated Tablet Philippines - English - FDA (Food And Drug Administration)

combizar 100mg/25mg film-coated tablet

sandoz philippines corporation; distributor: unilab, inc. - losartan potassium , hydrochlorothiazide - film-coated tablet - 100mg/25mg

BRONCOMAR- acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl liquid United States - English - NLM (National Library of Medicine)

broncomar- acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl liquid

gadal laboratories inc - acetaminophen (unii: 362o9itl9d) (acetaminophen - unii:362o9itl9d), dextromethorphan hydrobromide (unii: 9d2rti9kyh) (dextromethorphan - unii:7355x3rots), guaifenesin (unii: 495w7451vq) (guaifenesin - unii:495w7451vq), phenylephrine hydrochloride (unii: 04ja59tnsj) (phenylephrine - unii:1ws297w6mv) - purpose analgesic cough suppressant expectorant decongestant uses - for temporary relief of bronchial and nasal congestion - help loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes and make cough more productive. - teporarily relieves cough due to minor throat and bronchial irritation as may occur with the common cold do not use - if you are now taking a prescription monoamine oxidase inhibitor (maoi)( certain drugs for depression , psychiatric conditions, or parkinson’s disease) or for 2 weeks after stopping the maoi drug. - if you do not know if your prescription drug contains on maoi ask your doctor or pharmacist before taking this product - if you have a chronic pulmonary disease or shortness of breath unless directed by a doctor - avoid alcoholic beverages while you are taking this product - do not use with any other drug containing acetaminophen (prescirption or nonprescription). if you are not sure whether a drug contains acetaminophen, ask a doctor or a pharmacist. ask the

Combizar 100 mg / 25 mg Film-Coated Tablet Philippines - English - FDA (Food And Drug Administration)

combizar 100 mg / 25 mg film-coated tablet

unilab, inc.; importer: n/a; distributor: n/a - losartan potassium , hydrochlorothiazide - film-coated tablet - 100 mg / 25 mg

Combizar 100 mg/25 mg Film-Coated Tablet Philippines - English - FDA (Food And Drug Administration)

combizar 100 mg/25 mg film-coated tablet

n/a; importer: unilab, inc.; distributor: unilab, inc. - losartan potassium , hydrochlorothiazide - film-coated tablet - 100 mg/25 mg

BRONCOMAR MAXIMUN COUGH RELIEF- dextromethorphan hbr, guaifenesin liquid United States - English - NLM (National Library of Medicine)

broncomar maximun cough relief- dextromethorphan hbr, guaifenesin liquid

dannso corp./d.b.a. essential products - dextromethorphan hydrobromide (unii: 9d2rti9kyh) (dextromethorphan - unii:7355x3rots), guaifenesin (unii: 495w7451vq) (guaifenesin - unii:495w7451vq) - dextromethorphan hydrobromide 30 mg in 10 ml - uses: - helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes and make cough more productive. - temporarily relieves cough due to minor throat and bronchial irritation as may occur with the common cold. do not use - if you are now taking a prescription monoamine oxidase inhibitor (maoi) (certain drugs for depression, psychiatric conditions, or parkinson's disease) or for 2 weeks after stopping maoi drug. - if you do not know if your prescription drug contains maoi as your doctor or pharmacist before taking this product. - if you have a chronic pulmonary disease or shortness of breath unless directed by a doctor. - avoid alcoholic beverage while taking this product. - nervousness, dizziness or sleeplessness occurs. - cough persists more than 1 week, tends to recur or is accompanied by a fever, rash or persistent headache. a persistent cough may be signserious condition. other information: - each 10 mls contains: sodium 4 mg - store between 15 - 30 degrees celsius (59 - 86 fahrenhei