Label: AURUM HYPERICUM pellet
- NDC Code(s): 48951-1281-2
- Packager: Uriel Pharmacy Inc
- 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 January 23, 2024
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- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
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ACTIVE INGREDIENT
Active Ingredients: Avena (Oats) 3X, Hypericum (St. John’s Wort) 3X, Acidum phosphoricum (Orthophosphoric acid) 5X, Ignatia (St. Ignatius’ bean) 5X, Hepar (Bovine liver) 5X, Magnesium hydroxydatum (Magnesium hydroxide) 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
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
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WARNINGS
Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. Do not use if allergic to any ingredient. Contains traces of lactose. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AURUM HYPERICUM
aurum hypericum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-1281 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OAT (UNII: Z6J799EAJK) (OAT - UNII:Z6J799EAJK) OAT 3 [hp_X] HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB) HYPERICUM PERFORATUM 3 [hp_X] PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN) PHOSPHORIC ACID 5 [hp_X] STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (STRYCHNOS IGNATII SEED - UNII:1NM3M2487K) STRYCHNOS IGNATII SEED 5 [hp_X] MAMMAL LIVER (UNII: D0846624BI) (MAMMAL LIVER - UNII:D0846624BI) MAMMAL LIVER 5 [hp_X] MAGNESIUM (UNII: I38ZP9992A) (MAGNESIUM - UNII:I38ZP9992A) MAGNESIUM 5 [hp_X] APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z) APIS MELLIFERA 6 [hp_X] SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 7 [hp_X] GOLD TRICHLORIDE (UNII: 15443PR153) (GOLD CATION (3+) - UNII:7XM25QYI14) GOLD TRICHLORIDE 7 [hp_X] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) Product Characteristics Color white (white) Score no score Shape ROUND (round) Size 3mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-1281-2 1350 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(48951-1281)