Ingilterra - Ingliż - MHRA (Medicines & Healthcare Products Regulatory Agency)

g.r. lane health products ltd - paracetamol; codeine phosphate; phenylephrine hydrochloride; diphenhydramine hydrochloride; caffeine - oral tablet - 500mg ; 10mg ; 10mg ; 15mg ; 30mg

Malta - Ingliż - Medicines Authority

alliance pharmaceuticals limited - ascorbic acid; sodium ascorbate - chewable tablet - ascorbic acid 148.93 mg; sodium ascorbate 176.74 mg - vitamins

Malta - Ingliż - Medicines Authority

alliance pharma (ireland) ltd - ascorbic acid, sodium ascorbate - chewable tablet - ascorbic acid 148.93 milligram(s) ; sodium ascorbate 176.74 milligram(s) - vitamins

Malta - Ingliż - Medicines Authority

phoenix labs suite 12, bunkilla plaza, bracetown business park clonee, county meath d15 xc64 , ireland - ascorbic acid, sodium ascorbate - chewable tablet - ascorbic acid 148.93 mg sodium ascorbate 176.74 mg - vitamins

Irlanda - Ingliż - HPRA (Health Products Regulatory Authority)

wrafton laboratories ltd. t/a perrigo - guaifenesin; paracetamol; phenylephrine hydrochloride - tablet - 250/100/5 milligram(s) - anilides; paracetamol, combinations excl. psycholeptics

Awstralja - Ingliż - Department of Health (Therapeutic Goods Administration)

boucher & muir pty ltd - paracetamol, quantity: 10 mg/ml - injection, intravenous infusion - excipient ingredients: water for injections; mannitol; sodium hydroxide; dibasic sodium phosphate dihydrate; povidone - paracetamol bnm 1000mg/100ml, solution for infusion is indicated for the relief of mild to moderate pain and the reduction of fever where an intravenous route of administration is considered clinically necessary.

New Zealand - Ingliż - Medsafe (Medicines Safety Authority)

haleon new zealand ulc - guaifenesin 100mg;  ; paracetamol 250mg;  ;  ;  ; phenylephrine hydrochloride 5mg;  ;   - film coated tablet - active: guaifenesin 100mg   paracetamol 250mg       phenylephrine hydrochloride 5mg     excipient: colloidal silicon dioxide lactose monohydrate maize starch microcrystalline cellulose opadry white oy-ls-28913 potassium sorbate povidone pregelatinised maize starch purified talc purified water stearic acid - effective, temporary relief of pain and discomfort associated with cold & flu symptoms: headache, blocked or runny nose, painful sinuses, sore throat, chesty productive cough, shivers, aches and pains. reduces fever.

Malta - Ingliż - Medicines Authority

galpharm healthcare limited wrafton, braunton, north devon, ex33 2dl, united kingdom - paracetamol, phenylephrine hydrochloride - hard capsule - paracetamol 500 mg phenylephrine hydrochloride 12.18 mg - analgesics

Awstralja - Ingliż - Department of Health (Therapeutic Goods Administration)

sanofi-aventis australia pty ltd - paracetamol, quantity: 500 mg; codeine phosphate hemihydrate, quantity: 30 mg - tablet, uncoated - excipient ingredients: potassium sorbate; maize starch; povidone; purified talc; stearic acid; magnesium stearate; microcrystalline cellulose; croscarmellose sodium; pregelatinised maize starch - paracetamol/codeine gh 500/30 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.

Ingilterra - Ingliż - MHRA (Medicines & Healthcare Products Regulatory Agency)

reckitt benckiser healthcare (uk) ltd - caffeine; phenylephrine hydrochloride; paracetamol - oral capsule - 25mg ; 6.1mg ; 500mg