Ireland - English - HPRA (Health Products Regulatory Authority)

john wyeth & brother limited - ambutonium bromide magnesium hydroxide aluminium hydroxide gel -

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)

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.

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

sanofi - magnesium hydroxide; aluminium hydroxide gel dried - oral suspension - 39mg/1ml ; 44mg/1ml

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)

chattem, inc. - magnesium hydroxide (unii: nbz3qy004s) (magnesium cation - unii:t6v3lhy838) - magnesium hydroxide usp 600 mg........................................................................................saline laxative ● for relief of occasional constipation (irregularity) ● this product generally produces bowel movement in ½ to 6 hours

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

bryant ranch prepack - ammonium lactate (unii: 67m901l9nq) (lactic acid - unii:33x04xa5at) - 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)

bryant ranch prepack - ammonium lactate (unii: 67m901l9nq) (lactic acid - unii:33x04xa5at) - 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.