Label: AURUM HYPERICUM SPECIAL ORDER liquid

  • 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 May 3, 2018

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

  • INDICATIONS & USAGE

    Directions: FOR ORAL USE ONLY.

  • DOSAGE & ADMINISTRATION

    Take 3-4 times daily. Ages 12 and older: 10 drops.
    Ages 2-11: 5 drops. Under age 2: Consult a doctor.

  • ACTIVE INGREDIENT

    Active Ingredients: Avena (Oats) 3X, Hypericum (St. John’s Wort) 3X, Acidum phos. (Orthophosphoric acid) 5X, Hepar (Bovine liver) 5X, Magnesium hydroxydatum (Magnesium hydroxide) 5X, Ignatia (St. Ignatius’ bean) 5X, Apis regina (Queen Bee cell with larva and nutrient fluid) 6X, Amethyst (Nat. silicic acid anhydrate with traces of manganese and iron) 7X, Aurum chloratum (Tetrachloroauric acid) 7X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Distilled water, 20% Organic cane alcohol, Lactose

  • PURPOSE

    Use: Temporary relief of headache.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

  • WARNINGS

    Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. Contains traces of lactose. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.

  • QUESTIONS

    Questions? Call 866.642.2858
    Made with care by Uriel, East Troy, WI 53120
    www.urielpharmacy.com

  • PRINCIPAL DISPLAY PANEL

    AurumHypericumSOLiquid

  • INGREDIENTS AND APPEARANCE
    AURUM HYPERICUM SPECIAL ORDER 
    aurum hypericum special order liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-1294
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GOLD TRICHLORIDE (UNII: 15443PR153) (GOLD CATION (3+) - UNII:7XM25QYI14) GOLD TRICHLORIDE7 [hp_X]  in 1 mL
    MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM HYDROXIDE5 [hp_X]  in 1 mL
    STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (STRYCHNOS IGNATII SEED - UNII:1NM3M2487K) STRYCHNOS IGNATII SEED5 [hp_X]  in 1 mL
    ROYAL JELLY (UNII: L497I37F0C) (ROYAL JELLY - UNII:L497I37F0C) ROYAL JELLY6 [hp_X]  in 1 mL
    AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (AVENA SATIVA FLOWERING TOP - UNII:MA9CQJ3F7F) AVENA SATIVA FLOWERING TOP3 [hp_X]  in 1 mL
    PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN) PHOSPHORIC ACID5 [hp_X]  in 1 mL
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE7 [hp_X]  in 1 mL
    ST. JOHN'S WORT (UNII: UFH8805FKA) (ST. JOHN'S WORT - UNII:UFH8805FKA) ST. JOHN'S WORT3 [hp_X]  in 1 mL
    MAMMAL LIVER (UNII: D0846624BI) (MAMMAL LIVER - UNII:D0846624BI) MAMMAL LIVER5 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-1294-360 mL in 1 BOTTLE, DROPPER; 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 Inc.043471163manufacture(48951-1294)