Label: SILICA powder

  • 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 July 24, 2017

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

View All Sections
  • Purpose

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

  • 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.

  • 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

  • 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.

  • Keep out of reach of children

    KEEP OUT OF REACH OF CHILDREN.

  • 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.

  • Ask doctor section

    Consult your doctor if you are lactose intolerant.

  • Pregnancy or breast feeding section

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

  • Questions section

    Made with care by

    Uriel Pharmacy

    East Troy, WI 53120

    Questions or comments?

    Please call 1.866.642.2858

    www.urielpharmacy.com

  • Principal Display Panel

    SilicaPow

  • INGREDIENTS AND APPEARANCE
    SILICA 
    silica powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-8317
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z) (EQUISETUM ARVENSE TOP - UNII:1DP6Y6B65Z) EQUISETUM ARVENSE TOP5 [hp_X]
    WHITE OAK BARK (UNII: 93LP7Y8EGT) (WHITE OAK BARK - UNII:93LP7Y8EGT) WHITE OAK BARK9 [hp_X]
    MAMMAL LIVER (UNII: D0846624BI) (MAMMAL LIVER - UNII:D0846624BI) MAMMAL LIVER9 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE (UNII: J2B2A4N98G)  
    POLLEN (UNII: 3729L8MA2C)  
    ANISE OIL (UNII: 6Y89129C8H)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-8317-71 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product09/01/2009
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/01/2009
    Labeler - Uriel Pharmacy Inc (043471163)
    Establishment
    NameAddressID/FEIBusiness Operations
    Uriel Pharmacy Inc043471163manufacture(48951-8317)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!