Label: PARA-BN- parathyroid booster liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated December 28, 2023

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  • Para-BN

    Alfalfa 7X                                                            Croton Tiglium 6X

    Arsenicum Album 15X, 30X                                 Kali Carbonicum 10X

    Aurum Muriaticum Natronatum 15X, 20X            Magnesium Phosphoricum 10X

    Calcarea Caustica 20X                                       Podophyllum Peltatum 7X

    Calcarea Fluorica 12X                                        Teucrium Marum 10X

    Calcarea Iodata 12X                                         Uranium Nitricum 17X

    Calcarea Oxalica 15X, 20X

  • Para-BN

    Alcohol, Purified Water

  • Para-BN

    Use only under the direction of a health care professional. Do not use if tamper evident seal is broken or missing.

  • Para-BN

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

  • Para-BN

    For the temporary relief of pain and discomfort in joints and muscle cramping

  • Para-BN

    Orally 25 drops, 2 times per day or as indicated by a physician. Children 12 and under use one falf the adult dosage.

  • Para-BN

    For regulation of calcium absorption.

  • Para-BN

    Label

  • INGREDIENTS AND APPEARANCE
    PARA-BN 
    parathyroid booster liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64616-102
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALFALFA (UNII: DJO934BRBD) (ALFALFA - UNII:DJO934BRBD) ALFALFA7 [hp_X]  in 1 mL
    ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIOXIDE30 [hp_X]  in 1 mL
    SODIUM TETRACHLOROAURATE (UNII: 7FT6QUT299) (TETRACHLOROAURATE ION - UNII:ZNL6IP5PJX) SODIUM TETRACHLOROAURATE20 [hp_X]  in 1 mL
    CALCIUM HYDROXIDE (UNII: PF5DZW74VN) (HYDROXIDE ION - UNII:9159UV381P) CALCIUM HYDROXIDE20 [hp_X]  in 1 mL
    CALCIUM FLUORIDE (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O) CALCIUM FLUORIDE12 [hp_X]  in 1 mL
    CALCIUM IODIDE (UNII: 8EKI9QEE2H) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM IODIDE12 [hp_X]  in 1 mL
    CALCIUM OXALATE MONOHYDRATE (UNII: 4PP86KK527) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM OXALATE MONOHYDRATE20 [hp_X]  in 1 mL
    CROTON TIGLIUM SEED (UNII: 0HK2GZK66E) (CROTON TIGLIUM SEED - UNII:0HK2GZK66E) CROTON TIGLIUM SEED6 [hp_X]  in 1 mL
    POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) POTASSIUM CARBONATE10 [hp_X]  in 1 mL
    MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE10 [hp_X]  in 1 mL
    PODOPHYLLUM (UNII: 2S713A4VP3) (PODOPHYLLUM - UNII:2S713A4VP3) PODOPHYLLUM7 [hp_X]  in 1 mL
    TEUCRIUM MARUM (UNII: 10464S0TAA) (TEUCRIUM MARUM - UNII:10464S0TAA) TEUCRIUM MARUM10 [hp_X]  in 1 mL
    URANYL NITRATE HEXAHYDRATE (UNII: 3V057702FY) (URANIUM CATION (6+) - UNII:5PI36AS4G7) URANYL NITRATE HEXAHYDRATE17 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64616-102-0259 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product04/08/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic04/08/2013
    Labeler - Vitality Works, Inc. (137752817)
    Registrant - Vitality Works, Inc. (137752817)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vitality Works, Inc.137752817manufacture(64616-102)
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