Belgium - English - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

johnson & johnson consumer sa-nv - paracetamol 250 mg/5 ml - oral suspension - 50 mg/ml - paracetamol 50 mg/ml - paracetamol

United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

phoenix labs ltd - paracetamol - suppository - 250mg

New Zealand - English - Medsafe (Medicines Safety Authority)

douglas pharmaceuticals limited - paracetamol 50 mg/ml;   - oral suspension - 250 mg/5ml - active: paracetamol 50 mg/ml   excipient: ammonium glycyrrhizinate carbomer glycerol hydrochloric acid nipastat purified water raspberry sodium cyclamate sodium hydroxide sunset yellow fcf xanthan gum

New Zealand - English - Medsafe (Medicines Safety Authority)

douglas pharmaceuticals limited - paracetamol 50 mg/ml;   - oral solution - 250 mg/5ml - active: paracetamol 50 mg/ml   excipient: amaranth ammonium glycyrrhizinate citric acid glycerol macrogols potassium sorbate propylene glycol purified water raspberry sodium benzoate sodium cyclamate sorbitol as sorbitol 70% sunset yellow fcf

New Zealand - English - Medsafe (Medicines Safety Authority)

multichem nz limited - paracetamol 50 mg/ml;  ;   - oral suspension - 250 mg/5ml - active: paracetamol 50 mg/ml     excipient: acesulfame potassium citric acid monohydrate dispersible cellulose enhancer flavour sg 12088 glycerol methyl hydroxybenzoate orange delight os flavour 12101 propyl hydroxybenzoate purified water saccharin sodium sodium citrate dihydrate sorbitol sucralose sunset yellow fcf xanthan gum - for the temporary relief of mild to moderate pain and fever associated with cold and flu, teething, toothache, headache, earache, sore throat and immunisation.

Australia - English - 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 - English - Medsafe (Medicines Safety Authority)

pharmacy retailing (nz) ltd t/a healthcare logistics - paracetamol 50 mg/ml;   - oral suspension - 250 mg/5ml - active: paracetamol 50 mg/ml   excipient: ammonium glycyrrhizinate carbomer nature imitation raspberry no. 1 special qz04371 glycerol hydrochloric acid nipastat sodium cyclamate sodium hydroxide sunset yellow fcf water xanthan gum

New Zealand - English - Medsafe (Medicines Safety Authority)

douglas pharmaceuticals limited - paracetamol 50 mg/ml;   - oral solution - 250 mg/5ml - active: paracetamol 50 mg/ml   excipient: amaranth ammonium glycyrrhizinate citric acid glycerol macrogols as polyethylene glycol 1450 potassium sorbate propylene glycol purified water raspberry sodium benzoate sodium cyclamate sorbitol as sorbitol 70% sunset yellow fcf

New Zealand - English - Medsafe (Medicines Safety Authority)

douglas pharmaceuticals limited - paracetamol 50 mg/ml;   - oral suspension - 250 mg/5ml - active: paracetamol 50 mg/ml   excipient: ammonium glycyrrhizinate carbomer glycerol hydrochloric acid nipastat raspberry sodium cyclamate sodium hydroxide sunset yellow fcf water xanthan gum

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

aft pharmaceuticals pty ltd - paracetamol, quantity: 10 mg/ml - injection, intravenous infusion - excipient ingredients: hydrochloric acid; cysteine hydrochloride monohydrate; dibasic sodium phosphate dihydrate; mannitol; nitrogen; water for injections; sodium hydroxide - paracetamol-aft 10mg/ml, 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.