Label: BIPLA- sus scrofa placenta liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 52964-1001-1 - Packager: TMN K.K.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated August 2, 2012
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- 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
BIPLA
sus scrofa placenta liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52964-1001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SUS SCROFA PLACENTA (UNII: C8CV8867O8) (SUS SCROFA PLACENTA - UNII:C8CV8867O8) SUS SCROFA PLACENTA 16000 mg in 30 mL Inactive Ingredients Ingredient Name Strength ERYTHRITOL (UNII: RA96B954X6) TREHALOSE (UNII: B8WCK70T7I) APPLE JUICE (UNII: 9871T0PD5P) MALIC ACID (UNII: 817L1N4CKP) CARAMEL (UNII: T9D99G2B1R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52964-1001-1 30 mL in 1 BOTTLE, GLASS Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/02/2012 Labeler - TMN K.K. (711474452) Registrant - TMN K.K. (711474452) Establishment Name Address ID/FEI Business Operations TMN K.K. 711474452 manufacture(52964-1001)
