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  • Tsumura Choutousan[47] : 189 sachets
  • JP


Tsumura Choutousan[47] : 189 sachets

Sale Price:US$162.49

Warehouse Japan1
Manufacturer TSUMURA & CO.
JAN Code 4987138804730
GS1 14987138804737
Ingredient Code 5200101
Shipping Schedule 5 to 10 working days after payment


Chotosan is indicated for the relief of chronic headache with hypertension in those middle-aged or elderly.


189 sachets


light grayish brown granules

Active Ingredients

7.5 g (3sachets for 1day)of TSUMURA Chotosan extract granules contains 4.5 g of a dried extract of the following mixed crude drugs.JP Gypsum 5.0 gJP Uncaria Thorn 3.0 gJP Citrus Unshiu Peel 3.0 gJP Ophiopogon Tuber 3.0 gJP Pinellia Tuber 3.0 gJP Poria Sclerotium 3.0 gJP Chrysanthemum Flower 2.0 gJP Ginseng 2.0 gJP Saposhnikovia Root 2.0 gJP Glycyrrhiza 1.0 gJP Ginger 1.0 g(JP: The Japanese Pharmacopoeia)


TJ-47 is indicated for the relief of chronic headache with hypertension in those middle-aged or elderly.


The usual adult dose is 7.5 g/day orally in 2 or 3 divided doses before or between meals. The dosage may be adjusted according to the patient's age and body weight, and symptoms.


(1) When TJ-47 is used, the patient’s “SHO” (constitution/symptoms) should be taken into account. The patient’s progress should be carefully monitored, and if no improvement in symptoms/findings is observed, continuous treatment should be avoided.
(2) Since TJ-47 contains Glycyrrhiza, careful attention should be paid to the serum potassium level, blood pressure, etc., and if any abnormality is observed, administration should be discontinued.
(3) When TJ-47 is coadministered with other Kampo-preparations (Japanese traditional herbal medicines), etc., attention should be paid to the duplication of the contained crude drugs.

SHO: The term “SHO” refers to a particular pathological status of a patient evaluated by the Kampo diagnosis, and is patterned according to the patient’s constitution, symptoms, etc. Kampo-preparations (Japanese traditional herbal medicines) should be used after confirmation that it is suitable for the identified “SHO” of the patient.