Pharmaceutical composition for treating tinea pedis and preparation method thereof
A composition and drug technology, applied in the field of medicine, can solve problems such as side effects, sharp itching of feet, and low satisfaction, and achieve the effect of less side effects and less adverse reactions
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Embodiment 1
[0039] 1) The oil phase component raw materials of the following parts by weight are weighed and thrown into the oil phase container to obtain the oil phase mixture A: 8.0 kg of glyceryl monostearate and PEG-100 stearate, 5.0 kg of palm stearyl alcohol, 8.0 Kg of white oil, 0.6 kg of Pan 60, 3.0 kg of stearic acid, 2.0 kg of Melaleuca alternifolia oil, 1.0 kg of glyceryl monostearate, 0.2 kg of ethyl paraben, 0.1 kg of dibutyl hydroxytoluene;
[0040] Weigh the following water phase component raw materials into the water phase container to obtain the water phase mixture B: 2.5 kg of glycerin, 4.0 kg of potassium cetyl phosphate, 43.5 kg of purified water, 0.0004 kg of sodium citrate, 0.0001 kg of citric acid monohydrate;
[0041] Weigh the following parts by weight of the pharmaceutically active component raw materials and throw them into the pharmaceutically active component container to obtain the pharmaceutically active component mixture C: 9.0 kg of propylene glycol, 1.0 k...
Embodiment 2
[0047] 1) Weigh the following oil phase component raw materials into the oil phase container to obtain oil phase mixture A: 5.0 kg of glyceryl monostearate and PEG-100 stearate, 3.0 kg of palm stearyl alcohol, 5.0 Kg of white oil, 0.5 kg of Pan 60, 2.0 kg of stearic acid, 1.0 kg of Melaleuca alternifolia oil, 1.0 kg of glyceryl monostearate, 0.1 kg of ethyl paraben, 0.1 kg of dibutyl hydroxytoluene;
[0048] Weigh the following water phase component raw materials into the water phase container to obtain the water phase mixture B: 1.0 kg of glycerin, 2.0 kg of potassium cetyl phosphate, 45.0 kg of purified water, 0.0004 kg of sodium citrate, 0.0001 kg citric acid monohydrate;
[0049] Weigh the following parts by weight of the pharmaceutically active component raw materials and throw them into the pharmaceutically active component container to obtain the pharmaceutically active component mixture C: 5.0 kg of propylene glycol, 1.0 kg of menthol, 1.0 kg of camphor, 1.0 kg of born...
Embodiment 3
[0055] 1) Weigh the following oil phase component raw materials into the oil phase container to obtain oil phase mixture A: 10.0 kg of glyceryl monostearate and PEG-100 stearate, 10.0 kg of palm stearyl alcohol, 10.0 Kg of white oil, 1.0 kg of Pan 60, 5.0 kg of stearic acid, 4.0 kg of Melaleuca alternifolia oil, 3.0 kg of glyceryl monostearate, 0.2 kg of ethyl paraben, 0.2 kg of dibutyl hydroxytoluene;
[0056] Weigh the following water phase component raw materials into the water phase container to obtain the water phase mixture B: 5.0 kg of glycerin, 6.0 kg of potassium cetyl phosphate, 55.0 kg of purified water, 0.0004 kg of sodium citrate, 0.0001 kg of citric acid monohydrate;
[0057] Weigh the following parts by weight of the pharmaceutically active component raw materials and throw them into the pharmaceutically active component container to obtain the pharmaceutically active component mixture C: 10.0 kg of propylene glycol, 2.0 kg of menthol, 2.0 kg of camphor, 2.0 kg ...
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