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ECZEMA (HOMEOLAB USA INC.)

Available Formats

Dosage Form Package Information Links
TABLET, CHEWABLE 90 TABLET, CHEWABLE in 1 BOTTLE (60512-6009-0) Label Information

Complete ECZEMA Information

  • ACTIVE INGREDIENTS HPUS

    Fumaria officinalis (Common fumitory) 6C

    Natrum muriaticum (Salt) 6C

    Agaricus muscarius (Fly agaric) 6C

    Petroleum (Rock-oil) 6C

    Sepia (Sepia) 6C

    Kali arsenicosum (Potassium arsenite) 6C

    Alumina (Alumina) 6C


  • REFERENCES

    The letters 'HPUS' indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.


  • PURPOSE

    dry scaly skin

    dry and cracked skin, body rash

    itching and redness

    intense itching behind the ears, redness, dry and cracked skin

    itching

    dry skin and itching

    itching rash


  • USES

    This homeopathic medicine helps relieve symptoms of eczema:

    - dry skin

    - body rashes

    - cracked skin

    - itching


  • WARNINGS


    Stop use and ask a doctor if symptoms worsen or persist for more than 7 days.

    If pregnant or breast-feeding, ask a health professional before use.

    Keep out of reach of children.


  • DIRECTIONS

    Chew tablets and let dissolve in mouth.

    Do not use more than directed.

    Do not take with food.

    Repeat 3 times daily and reduce intake with improvement or as directed by a health professional.

    Age Dose
    Adults and children 12 years of age and older 2 tablets
    Children 2 to 11 years of age 1 tablet
    Children under 2 years of age Ask a doctor


  • OTHER INFORMATION

    Store at room temperature (68 - 77F).

    Do not use if seal is broken or missing.


  • INACTIVE INGREDIENTS

    Lactose, magnesium stearate.



  • CARTON

    image of carton label


  • INGREDIENTS AND APPEARANCE
    ECZEMA  REAL RELIEF
    fumaria officinalis, natrum muriaticum, agaricus muscarius, petroleum, sepia, kali arsenicosum, alumina tablet, chewable
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:60512-6009
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    FUMARIA OFFICINALIS FLOWERING TOP (UNII: VH659J61ZL) (FUMARIA OFFICINALIS FLOWERING TOP - UNII:VH659J61ZL) FUMARIA OFFICINALIS FLOWERING TOP 6 [hp_C]
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CATION 6 [hp_C]
    AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY (UNII: DIF093I037) (AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY - UNII:DIF093I037) AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY 6 [hp_C]
    KEROSENE (UNII: 1C89KKC04E) (KEROSENE - UNII:1C89KKC04E) KEROSENE 6 [hp_C]
    SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (SEPIA OFFICINALIS JUICE - UNII:QDL83WN8C2) SEPIA OFFICINALIS JUICE 6 [hp_C]
    POTASSIUM ARSENITE ANHYDROUS (UNII: BM2U42PAKI) (ARSENITE ION - UNII:N5509X556J) ARSENITE ION 6 [hp_C]
    ALUMINUM OXIDE (UNII: LMI26O6933) (ALUMINUM OXIDE - UNII:LMI26O6933) ALUMINUM OXIDE 6 [hp_C]
    Inactive Ingredients
    Ingredient Name Strength
    LACTOSE (UNII: J2B2A4N98G)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    Product Characteristics
    Color white Score no score
    Shape ROUND Size 8mm
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:60512-6009-0 90 in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 07/25/2012
    Labeler - HOMEOLAB USA INC. (202032533)
    Establishment
    Name Address ID/FEI Business Operations
    HOMEOLAB USA INC. 202032533 manufacture(60512-6009)