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

johnson & johnson pacific pty ltd - ammonium chloride, quantity: 25 mg/ml; diphenhydramine hydrochloride, quantity: 2.5 mg/ml - oral liquid, solution - excipient ingredients: sucrose; liquid glucose; citric acid monohydrate; allura red ac; menthol; brilliant blue fcf; saccharin sodium; sodium benzoate; purified water; glycerol; sodium citrate dihydrate; flavour - for the relief of cough and nasal congestion due to common cold.

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

johnson & johnson pacific pty ltd - ammonium chloride, quantity: 25 mg/ml; diphenhydramine hydrochloride, quantity: 2.5 mg/ml - oral liquid, solution - excipient ingredients: brilliant blue fcf; menthol; sucrose; sodium benzoate; allura red ac; sodium citrate dihydrate; liquid glucose; purified water; saccharin sodium; citric acid monohydrate; glycerol; flavour - for the relief of cough and nasal congestion due to common cold.

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

kardwi pharmaceuticals pty limited - ammonium chloride, quantity: 6.25 mg/ml; sodium citrate dihydrate, quantity: 2.5 mg/ml; theophylline, quantity: 4.2 mg/ml; ammonium bicarbonate, quantity: 6.25 mg/ml; camphor, quantity: 0.225 mg/ml; diphenhydramine hydrochloride, quantity: 1.25 mg/ml - oral liquid - excipient ingredients: purified water; sucrose; benzoic acid; anise oil; ethanol; liquorice; chloroform; glycerol; tolu balsam; acetic acid; purified honey; ammonia; methyl hydroxybenzoate; propyl hydroxybenzoate; amaranth - this product accepted for registration/listing as 'currently supplied' at the time of commencement of the act. indications held in artg paper records. (old code)

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

pharmacare laboratories pty ltd - menthol, quantity: 0.2 mg/ml; ammonium chloride, quantity: 25 mg/ml; sodium citrate dihydrate, quantity: 10 mg/ml; diphenhydramine hydrochloride, quantity: 2.5 mg/ml - oral liquid, solution - excipient ingredients: amaranth; caramel; glycerol; brilliant blue fcf; ethanol; sorbitol solution (70 per cent) (crystallising); propylene glycol; sucrose; purified water; propylene glycol alginate; flavour; methyl hydroxybenzoate; propyl hydroxybenzoate; ethyl hydroxybenzoate; butyl hydroxybenzoate; isobutyl hydroxybenzoate - for temporary relief of chesty coughs & head colds

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

arrow pharma pty ltd - menthol, quantity: 0.2 mg/ml; ammonium chloride, quantity: 25 mg/ml; sodium citrate dihydrate, quantity: 10 mg/ml; diphenhydramine hydrochloride, quantity: 2.5 mg/ml - oral liquid - excipient ingredients: glycerol; sorbitol solution (70 per cent) (non-crystallising); citric acid monohydrate; propylene glycol; sodium cyclamate; ethanol; purified water; sucrose; amaranth; flavour; propyl hydroxybenzoate; methyl hydroxybenzoate; ethyl hydroxybenzoate - relief of nasal and bronchial congestion. ease coughing.

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

nnodum pharmaceuticals - ammonium lactate (unii: 67m901l9nq) (lactic acid - unii:33x04xa5at) - ammonium lactate 17 g in 1 g - ammonium lactate cream is indicated for the treatment of dry, scaly skin (xerosis) and ichthyosis vulgaris and for temporary relief of itching associated with these conditions. ammonium lactate cream is contraindicated in those patients with a history of hypersensitivity to any of the label ingredients.

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

nnodum pharmaceuticals - ammonium lactate (unii: 67m901l9nq) (lactic acid - unii:33x04xa5at) - ammonium lactate 17 g in 1 g - ammonium lactate lotion is indicated for the treatment of dry, scaly skin (xerosis) and ichthyosis vulgaris and for temporary relief of itching associated with these conditions. ammonium lactate lotion is contraindicated in those patients with a history of hypersensitivity to any of the label ingredients.

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

physicians total care, inc. - ammonium lactate (unii: 67m901l9nq) (lactic acid, dl- - unii:3b8d35y7s4) - lactic acid, dl- 12 g in 100 g - ammonium lactate lotion, 12% is indicated for the treatment of dry, scaly skin (xerosis) and ichthyosis vulgaris, and for the temporary relief of itching associated with these conditions. ammonium lactate lotion, 12% is contraindicated in those patients with a history of hypersensitivity to any of the label ingredients.

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

padagis israel pharmaceuticals ltd - ammonium lactate (unii: 67m901l9nq) (lactic acid - unii:33x04xa5at) - lactic acid 12 g in 100 g - ammonium lactate cream, 12% is indicated for the treatment of ichthyosis vulgaris and xerosis. ammonium lactate cream, 12% is contraindicated in those patients with a history of hypersensitivity to any of the label ingredients.

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

padagis israel pharmaceuticals ltd - ammonium lactate (unii: 67m901l9nq) (lactic acid - unii:33x04xa5at) - lactic acid 12 g in 100 g - ammonium lactate lotion, 12% is indicated for the treatment of dry, scaly skin (xerosis) and ichthyosis vulgaris, and for the temporary relief of itching associated with these conditions. ammonium lactate lotion, 12% is contraindicated in those patients with a history of hypersensitivity to any of the label ingredients.