Label: CEBASHIN CAP.- forsythia suspensa fruit, lonicera japonica whole, mentha arvensis top, platycodon grandiflorus root, licorice, arctium lappa fruit, glycine max whole, lophatherum gracile top, schizonepeta tenufolia spike, saiga tatarica horn capsule
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Contains inactivated NDC Code(s)
NDC Code(s): 72850-0007-1, 72850-0007-2 - Packager: Chunwoo Pharmaceutical Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated January 31, 2022
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Directions
- Inactive ingredients
- Keep out of reach of children
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Warnings
Do not use if you are
- Children under 5 years old
Do not use if you have
- Galactose intolerance
- Lapp lactase deficiency
- Glucose-galactose malabsorption (this medicine contains lactose)
Ask a doctor before use if you
- have hypertension
- have a heart disease or a kidney disease
- a patient with edema
- pregnant or have a chance to pregnant
- a patient who has rashes, bloodshot, redness, itching, and etc. caused by medication
- a patient with significantly weakened stomachs
- an elderly person (in general, elderly people should take with care, such as reducing their dosage, as their physiological function has deteriorated)
- in a post-disease stage (am abnormal reaction can be easily seen and the symptoms can worsen)
- a patient who is being treated by a doctor or are taking other medications
Stop use and ask a doctor, pharmacist or health professionals if
- if there is no improvement in symptoms after taking it for a few days
- you have following symptoms after use:
- Pseudohyperaldosteronism: Reduced urine volume, swollen face, swollen hands and feet, heavy eyelids, firm hands, increased blood pressure, headache, and etc. (Mediciness with a maximum daily dose of 1g or more may develop hypoglycemia, blood pressure rise, low sodium body fluid, edema, weight gain, and etc. caused by pseydohyperaldosteronism if taken continuously for a long time. Therefore, make sufficient observations (measurement of serum potassium levels) and stop taking if there is any abnormality.)
-Myopathy: Myopathy (muscle disease) may occur as a result of hypokalemia, so take sufficient observation and stop taking if you find any abnormalities such as feeling helplessness, limb cramps, paralysis, and etc.
-Skin trouble: a rash, itch, bloodshot, and etc.
-Digestive system disorder: anorexia, stomach discomfort, nausea, vomiting, and etc.
Other Warnings
- do not take more than directed
- if children are to take this medicine, take it under the supervision of their guardian.
- when taken with potassium-containing agents, licorice-containing agents, glycirizinic acid or other related agents, loop diuretics (furosemide, ethacrynic acid), or thiazide diuretics (trichlormethiazide) and myopathy, it is likely to appear due to gastric aldosterone (pseudohyperaldosteronism) or hypokalemia
- If taken with other herbal medicines, be careful of overlapping of the crude medicines.
- In principle, you should not to take it continuously for a long time, but if it is necessary, consult with a doctor, herb doctor, dentist, pharmacist, or other health care professionals.
- Uses
- Cebashin Cap.
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INGREDIENTS AND APPEARANCE
CEBASHIN CAP.
forsythia suspensa fruit, lonicera japonica whole, mentha arvensis top, platycodon grandiflorus root, licorice, arctium lappa fruit, glycine max whole, lophatherum gracile top, schizonepeta tenufolia spike, saiga tatarica horn capsuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72850-0007 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FORSYTHIA SUSPENSA FRUIT (UNII: P4793M1ES5) (FORSYTHIA SUSPENSA FRUIT - UNII:P4793M1ES5) FORSYTHIA SUSPENSA FRUIT 710 mg in 10 g LICORICE (UNII: 61ZBX54883) (LICORICE - UNII:61ZBX54883) LICORICE 426 mg in 10 g PLATYCODON GRANDIFLORUS ROOT (UNII: 2DF0NS0O2Z) (PLATYCODON GRANDIFLORUS ROOT - UNII:2DF0NS0O2Z) PLATYCODON GRANDIFLORUS ROOT 426 mg in 10 g ARCTIUM LAPPA FRUIT (UNII: EA541308MV) (ARCTIUM LAPPA FRUIT - UNII:EA541308MV) ARCTIUM LAPPA FRUIT 356 mg in 10 g LONICERA JAPONICA WHOLE (UNII: UV4X7MQQ43) (LONICERA JAPONICA WHOLE - UNII:UV4X7MQQ43) LONICERA JAPONICA WHOLE 710 mg in 10 g MENTHA ARVENSIS TOP (UNII: 8J5Y2F7A5X) (MENTHA ARVENSIS TOP - UNII:8J5Y2F7A5X) MENTHA ARVENSIS TOP 426 mg in 10 g GLYCINE MAX WHOLE (UNII: NID9NUV93F) (GLYCINE MAX WHOLE - UNII:NID9NUV93F) GLYCINE MAX WHOLE 356 mg in 10 g SCHIZONEPETA TENUFOLIA SPIKE (UNII: 2FN3BA1MZE) (SCHIZONEPETA TENUFOLIA SPIKE - UNII:2FN3BA1MZE) SCHIZONEPETA TENUFOLIA SPIKE 284 mg in 10 g LOPHATHERUM GRACILE TOP (UNII: OY50I2L657) (LOPHATHERUM GRACILE TOP - UNII:OY50I2L657) LOPHATHERUM GRACILE TOP 284 mg in 10 g SAIGA TATARICA HORN (UNII: PU683NDA7H) (SAIGA TATARICA HORN - UNII:PU683NDA7H) SAIGA TATARICA HORN 22 mg in 10 g Inactive Ingredients Ingredient Name Strength LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) Product Characteristics Color red, white Score no score Shape CAPSULE Size 21mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72850-0007-2 1 in 1 BOX 01/12/2022 1 NDC:72850-0007-1 10 g in 1 CAPSULE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/12/2022 Labeler - Chunwoo Pharmaceutical Co., Ltd. (688729065) Registrant - Chunwoo Pharmaceutical Co., Ltd. (688729065) Establishment Name Address ID/FEI Business Operations Chunwoo Pharmaceutical Co., Ltd. 688729065 manufacture(72850-0007)