Label: OKCHEONWON- trichosanthes kirilowii root, pueraria lobata root, liriope muscari root, ophiopogon japonicus root, prunus mume fruit, astragalus mongholicus root, asian ginseng, licorice pill
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Contains inactivated NDC Code(s)
NDC Code(s): 72850-0008-1, 72850-0008-2, 72850-0008-3 - 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
Warnings
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 are
- a hypertensive
- a heart or kidney patient
- an edema patient
- a patient who is being treated by a doctor or taking other medications.
- an elderly person (in general, elderly people should take with care, such as reducing their dosage, as their physiological function has deteriorated.)
- a child (the safety of children's use is not established. (Less experience in use))
Stop use and ask a doctor, pharmacist or health professionals and bring this if 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.
- Liver disorder: jaundice, fatigue, and etc.
- Interstitial lung disease: difficult to breathe, fever, and etc. accompanied by a cough.
- Urinary system disorder: dysuria
- The autonomic system disorder: insomnia, excessive sweating, fast pulse, frequent urination, palpitations, feeling helplessness, excitement, and etc.
- If there is no improvement in symptoms after taking it for one month
Other Warnings
- do not take more than directed
- 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.
- it is easy to experience symptoms such as insomnia, hyperhidrosis, rapid pulse, frequent urination, palpitations, general fatigue, and mental excitement when use with Ephedra Sinica Stem or ephedrine-containing agents, MAO inhibitors, thyroid agents (thyroxine, liothyronine), catecholamine (epinephrine, isoprenaline) and xanthine agents (theophylline, diprophylline) so take it carefully, such as reducing the dose.
- Uses
- Okcheonwon
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INGREDIENTS AND APPEARANCE
OKCHEONWON
trichosanthes kirilowii root, pueraria lobata root, liriope muscari root, ophiopogon japonicus root, prunus mume fruit, astragalus mongholicus root, asian ginseng, licorice pillProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72850-0008 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LICORICE (UNII: 61ZBX54883) (LICORICE - UNII:61ZBX54883) LICORICE 13.9 mg in 10 g TRICHOSANTHES KIRILOWII ROOT (UNII: V409XGE0TS) (TRICHOSANTHES KIRILOWII ROOT - UNII:V409XGE0TS) TRICHOSANTHES KIRILOWII ROOT 20.8 mg in 10 g PUERARIA MONTANA VAR. LOBATA ROOT (UNII: PET93F4I3C) (PUERARIA MONTANA VAR. LOBATA ROOT - UNII:PET93F4I3C) PUERARIA MONTANA VAR. LOBATA ROOT 20.8 mg in 10 g LIRIOPE MUSCARI ROOT (UNII: 8PHD8TAO0Q) (LIRIOPE MUSCARI ROOT - UNII:8PHD8TAO0Q) LIRIOPE MUSCARI ROOT 13.9 mg in 10 g PRUNUS MUME FRUIT (UNII: 639190I8CU) (PRUNUS MUME FRUIT - UNII:639190I8CU) PRUNUS MUME FRUIT 13.9 mg in 10 g ASTRAGALUS MONGHOLICUS ROOT (UNII: 59DK50719X) (ASTRAGALUS MONGHOLICUS ROOT - UNII:59DK50719X) ASTRAGALUS MONGHOLICUS ROOT 13.9 mg in 10 g ASIAN GINSENG (UNII: CUQ3A77YXI) (ASIAN GINSENG - UNII:CUQ3A77YXI) ASIAN GINSENG 13.9 mg in 10 g OPHIOPOGON JAPONICUS ROOT (UNII: 90PS6JV9GZ) (OPHIOPOGON JAPONICUS ROOT - UNII:90PS6JV9GZ) OPHIOPOGON JAPONICUS ROOT 13.9 mg in 10 g Inactive Ingredients Ingredient Name Strength LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) Product Characteristics Color brown Score no score Shape ROUND Size 5mm Flavor Imprint Code None Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72850-0008-3 1 in 1 BOX 01/12/2022 1 NDC:72850-0008-2 30 in 1 CASE 1 NDC:72850-0008-1 15 g in 1 BLISTER PACK; 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(72850-0008)