Label: SILICA- silica powder

  • Category: HUMAN OTC DRUG LABEL

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 July 24, 2017

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • Purpose

    Uses: To promote skin elasticity and strengthen hair and nails.

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  • Dosage & Administration

    Directions: Take regularly before meals with a small amount of water. Ages 12 and older: 1 tsp. Ages 2-11: 1/2 tsp.   Under age 2: Ask a doctor.

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  • OTC-Active Ingredient

    Active Ingredients: Stannum met. (Metallic tin) 3X, Cinis equiseti (Ash of horsetail herb) 5X, Cinis quercus (Decoction of oak bark ash) 9X, Cor (Bovine heart) 9X, Hepar (Bovine liver) 9X, Pancreas (Bovine pancreas) 9X, Pulmo (Bovine lung) 9X, Quercus (Oak) 9X, Renes (Bovine kidneys) 9X, Mesenchyme (Porcine embryonic connective tissue) 11X

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  • Uses: To promote skin elasticity and strengthen hair and nails.
  • Inactive Ingredient

    Inactive Ingredients: Lactose, Bee pollen, Diatomaceous earth, Anise oil, Mesenchyme, Pancreas, Pulmo, Cor,  Renes.

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  • Keep out of reach of children

    KEEP OUT OF REACH OF CHILDREN.

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  • Do not use if allergic to any ingredient. Do not use if safety seal is broken or missing.

    Warnings:   Do not use if allergic to any ingredient. Do not use if safety seal is broken or missing.

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  • Ask doctor section

    Consult your doctor if you are lactose intolerant.

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  • Pregnancy or breast feeding section

    If you are pregnant or nursing, consult a doctor before use.

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  • Questions section

    Made with care by

    Uriel Pharmacy

    East Troy, WI 53120

    Questions or comments?

    Please call 1.866.642.2858

    www.urielpharmacy.com

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  • Principal Display Panel
  • INGREDIENTS AND APPEARANCE
    SILICA 
    silica powder
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-8317
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z) (EQUISETUM ARVENSE TOP - UNII:1DP6Y6B65Z) EQUISETUM ARVENSE TOP 5 [hp_X]
    WHITE OAK BARK (UNII: 93LP7Y8EGT) (WHITE OAK BARK - UNII:93LP7Y8EGT) WHITE OAK BARK 9 [hp_X]
    MAMMAL LIVER (UNII: D0846624BI) (MAMMAL LIVER - UNII:D0846624BI) MAMMAL LIVER 9 [hp_X]
    Inactive Ingredients
    Ingredient Name Strength
    LACTOSE (UNII: J2B2A4N98G)  
    POLLEN (UNII: 3729L8MA2C)  
    ANISE OIL (UNII: 6Y89129C8H)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:48951-8317-7 1 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/01/2009
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 09/01/2009
    Labeler - Uriel Pharmacy Inc (043471163)
    Establishment
    Name Address ID/FEI Business Operations
    Uriel Pharmacy Inc 043471163 manufacture(48951-8317)
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