“Kracie” Kampo Keishibukuryoganryo Extract Tablets (48 tablets)

Ingredients

The daily dose of 6 tablets (310 mg/tablet) contains 1,150 mg of Keishibukuryogan extract from the following mixed crude drugs;
Cinnamon Bark 2.0 g, Poria Sclerotium 2.0 g, Moutan Bark 2.0 g, Peach Kernel 2.0 g, Peony Root 2.0 g.
As inactive ingredients, this medicine contains Hydroxypropylcellulose, Croscarmellose Sodium, Magnesium Stearate, Silicon Dioxide, and Cellulose.

(Precautions relating to Ingredients)
Due to this medicine's use of extract from natural ingredients (crude drugs), there may be slight color variations between tablets. Also, there may be visible white areas on the tablet's surface, which are from additives.
And due to the use of extract including crude drug essential oil components (components that produce a scent), there may be a scent characteristic of kampo (traditional Chinese medicine).

Indications

Following symptoms in persons with adequate physical strength who sometimes complain of lower abdominal pain, stiff shoulders, heavy head, dizziness, hot flashes, and/or over-sensitiveness of feet to cold: Menstrual irregularity, menstrual disorders, menstrual pain, menopausal disorders, chi-no-michi-sho*, stiff shoulders, dizziness, heavy head, bruises (contusion), chilblains, spots on the skin, eczema/dermatitis, and acne. *Chi-no-michi-sho is a generic term for neuropsychiatric symptoms such as anxiety and irritation, and physical symptoms due to fluctuation of female hormones caused by menstruation, pregnancy, childbirth, and menopause.

Dosage and administration

Take the following dosages 3 times a day with water or warm water before or between meals.
Adults (15 years and over) - 2 tablets
14 - 7 years - 1 tablets
Less than 7 years - Do not use

(Precautions of Dosage and Administration)
When allowing children to take the medicine, a guardian must be present to watch and tell such them how to take it.

Precautions for use

Consultation
1. The following persons should contact a physician, pharmacist, or registered salesperson for a consultation before administration.
(1) Patients undergoing medical treatment from a physician.
(2) Pregnant women or women suspected of being pregnant.
(3) Persons who is physically weak (declining of physical strength or constitutional weakness).
(4) Patients who have experienced rash/redness, itching, etc. with drugs, etc.
2. If the following symptoms are observed after taking this drug, these may be adverse reactions, so immediately discontinue the use of this drug, and show this document to your physician, pharmacist, or registered salesperson for a consultation.
Affected areas: Symptoms
Skin: Rash/redness, itching
Gastrointestinal system: Loss pf apetite
The following serious symptoms may occur in rare cases, immediately seek medical aid.
Symptom names: Symptoms
Hepatic function failure: Symptoms, such as fever, itching, rash, jaundice (yellowing of skin and white of eyes), brown urine, general malaise, loss of appetite, etc. may occur.
3. The following symptoms may be observed after taking this drug. If these symptoms persist or worsen, discontinue the use of this drug, and show this document to your physician, pharmacist, or registered salesperson for a consultation.
Diarrhea
4. When symptoms do not improve even after taking the medicine for about 1 month (for about 1 week if you take this medicine for baby's night crying, and constipation), stop taking this medicine and consult a physician, pharmacist or registered salesperson, being sure to take this instruction leaflet with you.