Label: FERRUM PHOS- ferrum phos gel

  • NDC Code(s): 15631-2314-0, 15631-2314-1, 15631-2314-2, 15631-2314-3
  • Packager: Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
  • 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 March 30, 2016

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

  • ACTIVE INGREDIENT

    FERRUM PHOS GEL 1X HPUS

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  • USES

    Inflammation, swellings, relieves congestion and pain

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  • INDICATIONS

    Condition listed above or as directed by the physician

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  • DOSAGE & ADMINISTRATION SECTION

    Apply a thin layer of Gel to the affected area, repeat 3 times a day or as needed.

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  • WARNINGS

    This product is to be used for self-limiting conditions

    If symptoms do not improve in 4 days, or worsen, discontinue use and seek assistance of health professional

    As with any drug, if you are preganant, or nursing a baby, seek professional advice before taking this product

    Keep this and all medication out of reach of children

    Do not use if capseal is broken or missing.
    Close the cap tightly after use.

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  • INACTIVE INGREDIENTS

    ALOE VERA GEL

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  • STORAGE

    Store in a cool dark place

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  • QUESTIONS OR COMMENTS

    www.Rxhomeo.com | 1.888.2796642 | info@rxhomeo.com

    Rxhomeo, Inc 9415 Burnet Road, Suite 312, Austin, TX 78758

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  • INGREDIENTS AND APPEARANCE
    FERRUM PHOS 
    ferrum phos gel
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:15631-2314
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (FERROSOFERRIC PHOSPHATE - UNII:91GQH8I5F7) FERROSOFERRIC PHOSPHATE 1 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:15631-2314-0 1 in 1 CONTAINER 03/30/2016
    1 50 g in 1 CONTAINER; Type 0: Not a Combination Product
    2 NDC:15631-2314-1 1 in 1 CONTAINER 03/30/2016
    2 100 g in 1 CONTAINER; Type 0: Not a Combination Product
    3 NDC:15631-2314-2 1 in 1 CONTAINER 03/30/2016
    3 200 g in 1 CONTAINER; Type 0: Not a Combination Product
    4 NDC:15631-2314-3 1 in 1 CONTAINER 03/30/2016
    4 500 g in 1 CONTAINER; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 03/30/2016
    Labeler - Rxhomeo Private Limited d.b.a. Rxhomeo, Inc (650833994)
    Establishment
    Name Address ID/FEI Business Operations
    Rxhomeo Private Limited d.b.a. Rxhomeo, Inc 650833994 manufacture(15631-2314) , label(15631-2314)
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