Label: BONEARTH CARE- achyranthes bidentata blume liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 82230-0001-1 - Packager: Dong woo dang pharmacy Co.,Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated September 10, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BONEARTH CARE
achyranthes bidentata blume liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82230-0001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACHYRANTHES BIDENTATA WHOLE (UNII: 0B5LIZ2V2H) (ACHYRANTHES BIDENTATA WHOLE - UNII:0B5LIZ2V2H) ACHYRANTHES BIDENTATA WHOLE 3 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:82230-0001-1 100 mL in 1 POUCH; Type 0: Not a Combination Product 09/11/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/11/2021 Labeler - Dong woo dang pharmacy Co.,Ltd. (687094912) Registrant - Dong woo dang pharmacy Co.,Ltd. (687094912) Establishment Name Address ID/FEI Business Operations Dong woo dang pharmacy Co.,Ltd. 687094912 manufacture(82230-0001)