NDC | 71291-0001-1 |
Set ID | 4a476852-094f-3269-e054-00144ff88e88 |
Category | HUMAN OTC DRUG LABEL |
Packager | GEOLIM Pharmaceutical CO., Ltd. (Busan Branch) |
Generic Name | |
Product Class | |
Product Number | |
Application Number |
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
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INDICATIONS & USAGE
• Wild Cultivated Ginseng Purified Pharmacopuncture is prescription drug of a oriental medical doctor.
5 - 100 ml (usually 10 ml) of the Wild Cultivated Ginseng Purified Pharmacopuncture is intravenous
injection.
• In case of a patient who has a serious illness after the treatment of a oriental medical doctor,
administer 1 Oml once every 3 days or once a week for a general patient by intravenous injection.
• In winter season, Wild Cultivated Ginseng Purified Pharmacopuncture injcetion temperature is 37.5
degrees, and gradually injected into for 3 minutes. -
WARNINGS
• Wild Cultivated Ginseng Purified Pharmacopuncture is prescription medicine which can be used safely
only under prescription and supervision of oriental medicine doctor.
• A oriental medicine doctor or medical license doctor can use Wild Cultivated Ginseng Purified
Pharmacopuncture according to prescription.
• If you have serious illness talk to your doctor.
• Talk to your doctor about hypersensitivity reactions after Wild Cultivated Ginseng Purified
Pharmacopuncture injection.
• The expiration date is one year from the preparation date. - DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
WILD CULTIVATED GINSENG PURIFIED PHARMACOPUNCTURE
wild cultivated ginseng liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71291-0001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASIAN GINSENG (UNII: CUQ3A77YXI) (ASIAN GINSENG - UNII:CUQ3A77YXI) ASIAN GINSENG 1 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71291-0001-1 10 mL in 1 VIAL; Type 0: Not a Combination Product 02/01/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 02/01/2017 Labeler - GEOLIM Pharmaceutical CO., Ltd. (Busan Branch) (689851661) Registrant - GEOLIM Pharmaceutical CO., Ltd. (Busan Branch) (689851661) Establishment Name Address ID/FEI Business Operations GEOLIM Pharmaceutical CO., Ltd. (Busan Branch) 689851661 label(71291-0001) , manufacture(71291-0001) , pack(71291-0001)