Label: SOMA ANTI-CANCERGEN - asian ginseng powder
- NDC Code(s): 58370-1001-1
- Packager: SOMA Biotechnology Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
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- ACTIVE INGREDIENT
red ginseng powder
- INACTIVE INGREDIENT
coriolus versicolorr, licorice, aralia continentalis, houttuynia cortata, cnidium officinale, cinnamon bark, houttuynia, mulberry leaf, astragalus membranaceus, gigantic angelica, sweet rush, pepper, bongchul, plueropterus multiflorus, dired clove, caramel
To help the treatment of cancer, leukemia and brain tumor
- KEEP OUT OF REACH OF CHILDREN
keep out of reach of the children
- INDICATIONS & USAGE
■ Take 2 times a day (immediately after having breakfast and dinner.)
■ Adults: 5~7 tablets
■ Seniors: 3~5 tablets
■ Children: 1~3 tablets
■ If you have a cardiac disorder or cerebrovascular disease or you are a long-term medicated patient, gradually increase/reduce the dosage from 1 to 3 tablets with a week interval.
■ Ask a doctor before you take more than 8 tablets.
■ Do not exceed 8 tablets if you do not know your constitution
- DOSAGE & ADMINISTRATION
for oral use only
- INGREDIENTS AND APPEARANCE
asian ginseng powder
Product Information Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:58370-1001 Route of Administration ORAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASIAN GINSENG (ASIAN GINSENG) ASIAN GINSENG 5.67 g in 100 g Inactive Ingredients Ingredient Name Strength TRAMETES VERSICOLOR FRUITING BODY GLYCYRRHIZA GLABRA ARALIA CORDATA ROOT HOUTTUYNIA CORDATA FLOWERING TOP CNIDIUM OFFICINALE WHOLE CINNAMON MORUS AUSTRALIS LEAF ASTRAGALUS PROPINQUUS ROOT ANGELICA SINENSIS ROOT ACORUS GRAMINEUS ROOT PEPPERS ZEDOARY POLYGONUM CUSPIDATUM WHOLE CLOVE CARAMEL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58370-1001-1 75 g in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/06/2013 Labeler - SOMA Biotechnology Co., Ltd (688387576) Registrant - SOMA Biotechnology Co., Ltd (688387576) Establishment Name Address ID/FEI Business Operations SOMA Biotechnology Co., Ltd 688387576 manufacture(58370-1001)