Label: AURUM HYPERICUM liquid
- NDC Code(s): 48951-1190-1
- Packager: Uriel Pharmacy 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 April 17, 2018
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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, Hepar (Bovine liver)4X, Magnesium hydroxydatum (Magnesium hydroxide) 4X, Acidum phos. (Orthophosphoric acid) 5X, Ignatia (St. Ignatius' bean) 5X, Apis regina (Queen Bee cell with larvae and nutrient fluid) 6X, Aurum chloratum (Tetrachloroauric acid) 7X, Amethyst (Nat. silicic acid anhydrate with traces of manganese and iron) 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. 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.
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INGREDIENTS AND APPEARANCE
AURUM HYPERICUM
aurum hypericum liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-1190 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (AVENA SATIVA FLOWERING TOP - UNII:MA9CQJ3F7F) AVENA SATIVA FLOWERING TOP 3 [hp_X] in 1 mL ST. JOHN'S WORT (UNII: UFH8805FKA) (ST. JOHN'S WORT - UNII:UFH8805FKA) ST. JOHN'S WORT 3 [hp_X] in 1 mL MAMMAL LIVER (UNII: D0846624BI) (MAMMAL LIVER - UNII:D0846624BI) MAMMAL LIVER 4 [hp_X] in 1 mL MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM HYDROXIDE 4 [hp_X] in 1 mL PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN) PHOSPHORIC ACID 5 [hp_X] in 1 mL STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (STRYCHNOS IGNATII SEED - UNII:1NM3M2487K) STRYCHNOS IGNATII SEED 5 [hp_X] in 1 mL ROYAL JELLY (UNII: L497I37F0C) (ROYAL JELLY - UNII:L497I37F0C) ROYAL JELLY 6 [hp_X] in 1 mL GOLD TRICHLORIDE (UNII: 15443PR153) (GOLD CATION (3+) - UNII:7XM25QYI14) GOLD TRICHLORIDE 7 [hp_X] in 1 mL SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 7 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM CHLORIDE (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-1190-1 10 in 1 BOX 09/01/2009 1 1 mL in 1 AMPULE; Type 0: Not a Combination Product 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(48951-1190)