Label: YOBISIN- rehmannia root, angelica gigas root tablet
- NDC Code(s): 72988-0012-1
- Packager: Lydia Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated December 16, 2023
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- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
YOBISIN
rehmannia root, angelica gigas root tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72988-0012 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RHUBARB (UNII: G280W4MW6E) (RHUBARB - UNII:G280W4MW6E) RHUBARB 16.7 mg REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ) (REHMANNIA GLUTINOSA ROOT - UNII:1BEM3U6LQQ) REHMANNIA GLUTINOSA ROOT 416.7 mg ANGELICA GIGAS ROOT (UNII: 32766B2FHX) (ANGELICA GIGAS ROOT - UNII:32766B2FHX) ANGELICA GIGAS ROOT 416.7 mg AKEBIA STEM (UNII: 531B9G152H) (AKEBIA STEM - UNII:531B9G152H) AKEBIA STEM 416.7 mg SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) (SCUTELLARIA BAICALENSIS ROOT - UNII:7J95K7ID2S) SCUTELLARIA BAICALENSIS ROOT 250 mg LICORICE (UNII: 61ZBX54883) (LICORICE - UNII:61ZBX54883) LICORICE 125 mg ALISMA PLANTAGO-AQUATICA ROOT (UNII: 6DXR2088WL) (ALISMA PLANTAGO-AQUATICA ROOT - UNII:6DXR2088WL) ALISMA PLANTAGO-AQUATICA ROOT 250 mg FORSYTHIA SUSPENSA FRUIT (UNII: P4793M1ES5) (FORSYTHIA SUSPENSA FRUIT - UNII:P4793M1ES5) FORSYTHIA SUSPENSA FRUIT 16.7 mg PLANTAGO SEED (UNII: 9C60Y73166) (PLANTAGO SEED - UNII:9C60Y73166) PLANTAGO SEED 250 mg GINGER (UNII: C5529G5JPQ) (GINGER - UNII:C5529G5JPQ) GINGER 16.7 mg CHINESE CINNAMON (UNII: WS4CQ062KM) (CHINESE CINNAMON - UNII:WS4CQ062KM) CHINESE CINNAMON 16.7 mg Inactive Ingredients Ingredient Name Strength MAGNESIUM STEARATE (UNII: 70097M6I30) Product Characteristics Color brown Score no score Shape ROUND Size 10mm Flavor Imprint Code T;2 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72988-0012-1 20 in 1 PACKAGE; Type 0: Not a Combination Product 04/24/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/22/2019 Labeler - Lydia Co., Ltd. (695735569) Registrant - Lydia Co., Ltd. (695735569) Establishment Name Address ID/FEI Business Operations I World Pharmaceutical Co., Ltd. 688222857 manufacture(72988-0012) Establishment Name Address ID/FEI Business Operations Lydia Co., Ltd. 695735569 label(72988-0012)