Label: TOTAL CADMIUM- cadmium sulphuratum liquid

  • NDC Code(s): 61657-0958-1
  • Packager: White Manufacturing Inc. DBA Micro West
  • 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 August 25, 2014

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    CADMIUM SULPHURATUM [HPUS]  12X, 30X, 200C, 1M

    Contains equal volumes of each ingredient

  • PURPOSE

    For the temporary relief of difficult swallowing, sore liver, and sleep apnea

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • INDICATIONS

    INDICATIONS: For the temporary relief of difficult swallowing, sore liver, and sleep apnea

  • WARNING

    WARNING: STOP USE AND CALL A DOCTOR if symptoms persist or worsen. CONTAINS ALCOHOL: in case of accidental overdose, consult a poison control center immediately

    OTHER INFORMATION: Tamper resistant for your protection. Use only if safety seal is intact.

  • Pregnancy or Breast-feeding

    IF PREGNANT OR BREAST FEEDING, consult a healthcare professional before use.

  • DIRECTIONS

    DIRECTIONS: Take 6 drops orally, 4 times a day. For ages 2 to adult

  • INACTIVE INGREDIENTS

    Alcohol 20% v/v

    Purified water

  • MANUFACTURE

    MANUFACTURED FOR

    MICRO WEST

    P.O. Box 950

    DOUGLAS, WY 82633

    1-307-358-5066

  • LABEL

    IMAGE OF BOTTLE LABEL

  • INGREDIENTS AND APPEARANCE
    TOTAL CADMIUM 
    cadmium sulphuratum liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61657-0958
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CADMIUM SULFIDE (UNII: 057EZR4Z7Q) (CADMIUM CATION - UNII:T494FZ4G8G) CADMIUM SULFIDE12 [hp_X]  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61657-0958-130 mL in 1 BOTTLE, DROPPER
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/01/2011
    Labeler - White Manufacturing Inc. DBA Micro West (082307831)
    Establishment
    NameAddressID/FEIBusiness Operations
    King Bio Inc617901350manufacture(61657-0958) , pack(61657-0958) , label(61657-0958)