Label: CORPUS CALLOSUM granule

  • 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 September 27, 2023

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  • ACTIVE INGREDIENT

    Active Ingredient

    CORPUS CALLOSUM 200K GR

    CORPUS CALLOSUM 30K GR

    CORPUS CALLOSUM 4CH GR

    CORPUS CALLOSUM 6CH GR

    CORPUS CALLOSUM 7CH GR

    CORPUS CALLOSUM 9CH GR

  • PURPOSE

    Indications

    Helps maintain mental alertness and sharpness

  • WARNINGS

    Warning:
    If pregnant or breastfeeding, ask a health professional before use.
    Keep out of reach of children.
    In case of overdose, get medical help or contact a Poison Control Center right away.

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breastfeeding, ask a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • OVERDOSAGE

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

  • INACTIVE INGREDIENT

    Inactive Ingredients
    Lactose,
    sucrose.

  • DOSAGE & ADMINISTRATION

    Directions
    Adults: Take five granules three times daily or as recommended by your healthcare practitioner.
    Children: Take three granules and follow adult directions.

  • QUESTIONS

    QUESTIONS? 1-888-737-6925.

  • INDICATIONS & USAGE

    Indications

    Helps maintain mental alertness and sharpness

    Directions
    Adults: Take five granules three times daily or as recommended by your healthcare practitioner.
    Children: Take three granules and follow adult directions.

  • PRINCIPAL DISPLAY PANEL

    62106-6982

    UNDA
    Do not use if label perforation is broken
    Homeopathic Remedy
    NDC : 62106-6982-4
    CORPUS CALLOSUM
    Corpus callosum
    140 granules
    Indications

    Helps maintain mental alertness and sharpness

  • INGREDIENTS AND APPEARANCE
    CORPUS CALLOSUM 
    corpus callosum granule
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62106-6982
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ORYCTOLAGUS CUNICULUS WHOLE (UNII: 768BE616L8) (ORYCTOLAGUS CUNICULUS WHOLE - UNII:768BE616L8) ORYCTOLAGUS CUNICULUS WHOLE6 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE (UNII: J2B2A4N98G)  
    SUCROSE (UNII: C151H8M554)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62106-6982-410 in 1 CARTON03/25/201505/31/2024
    1140 in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic03/25/201505/31/2024
    Labeler - Seroyal USA (018361118)
    Establishment
    NameAddressID/FEIBusiness Operations
    SAN’UP401010287manufacture(62106-6982)
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