ECZEMA RELIEF (NATRUM MURIATICUM, AGARICUS MUSCARIUS, PETROLEUM, SEPIA, KALI ARSENICOSUM, ALUMINA) PELLET [HOMEOLAB USA INC.]

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  • ECZEMA RELIEF (NATRUM MURIATICUM, AGARICUS MUSCARIUS, PETROLEUM, SEPIA, KALI ARSENICOSUM, ALUMINA) PELLET [HOMEOLAB USA INC.]

ECZEMA RELIEF (NATRUM MURIATICUM, AGARICUS MUSCARIUS, PETROLEUM, SEPIA, KALI ARSENICOSUM, ALUMINA) PELLET [HOMEOLAB USA INC.]
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NDC 60512-0002-1
Set ID 16ec3734-3948-49b3-b451-cf52e8db03cb
Category HUMAN OTC DRUG LABEL
Packager HOMEOLAB USA INC.
Generic Name
Product Class
Product Number
Application Number
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  • ACTIVE INGREDIENTS HPUS

    Natrum muriaticum 6C

    Agaricus muscarius 6C

    Petroleum 6C

    Sepia 6C

    Kali arsenicosum 6C

    Alumina 6C

  • REFERENCES

    Manufactured according to the Homeopathic Pharmacopoeia of the United States (HPUS)

  • PURPOSE

    Eczema

  • USES

    This is a natural Homeopathic remedy that relieves:

    • eczema
  • WARNINGS

  • ASK DOCTOR

    If symptoms persist or worsen, discontinue use and contact a health professional.

  • PREGNANCY OR BREAST FEEDING

    As with any drug, if you are pregnant or nursing a baby, seek the advice of a health professional before using this product.

  • KEEP OUT OF REACH OF CHILDREN

    Keep this and all medications out of reach of children.

  • DIRECTIONS

    Adults: Allow 3 to 4 pellets to dissolve in mouth three times a day for 2 months.

    Children under 12: Take 1/2 the adult dose.

    Do not exceed recommended dosage.

  • OTHER INFORMATION

    Do not use if cap seal is broken.

    Homeolab USA Inc., 3025 De L'Assomption Blvd., Montreal, QC H1N 2H2  Canada

    PRODUCT OF CANADA

  • INACTIVE INGREDIENTS

    Lactose, sucrose

  • CARTON

    IMAGE OF CARTONIMAGE OF LABEL

  • INGREDIENTS AND APPEARANCE
    ECZEMA RELIEF 
    natrum muriaticum, agaricus muscarius, petroleum, sepia, kali arsenicosum, alumina pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60512-0002
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE6 [hp_C]
    AMANITA MUSCARIA WHOLE (UNII: RQ7YY49K9Q) (AMANITA MUSCARIA WHOLE - UNII:RQ7YY49K9Q) AMANITA MUSCARIA WHOLE6 [hp_C]
    KEROSENE (UNII: 1C89KKC04E) (KEROSENE - UNII:1C89KKC04E) KEROSENE6 [hp_C]
    SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (SEPIA OFFICINALIS JUICE - UNII:QDL83WN8C2) SEPIA OFFICINALIS JUICE6 [hp_C]
    POTASSIUM ARSENITE ANHYDROUS (UNII: BM2U42PAKI) (ARSENITE ION - UNII:N5509X556J) POTASSIUM ARSENITE ANHYDROUS6 [hp_C]
    ALUMINUM OXIDE (UNII: LMI26O6933) (ALUMINUM OXIDE - UNII:LMI26O6933) ALUMINUM OXIDE6 [hp_C]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    LACTOSE (UNII: J2B2A4N98G)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize4mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60512-0002-180 in 1 TUBE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic10/18/2013
    Labeler - HOMEOLAB USA INC. (202032533)
    Establishment
    NameAddressID/FEIBusiness Operations
    HOMEOLAB USA INC.202032533manufacture(60512-0002)
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