Aurum Hypericum
- Manufacturer
- Uriel Pharmacy, Inc
- Effective date
- 2025-02-12
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:34:57
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
INDICATIONS & USAGE SECTION
Directions: FOR ORAL USE.
DOSAGE & ADMINISTRATION SECTION
Take the contents of one ampule under the
tongue and hold for 30 seconds, then swallow.
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients: Avena (Oats) 3X, Hypericum (St. John's Wort) 3X, Hepar oryctolagus (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 SECTION
Inactive Ingredients: Water, Salt, Lactose
Prepared using rhythmical processes.
OTC - PURPOSE SECTION
Uses: Temporary relief of depressed mood and nervous exhaustion.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
KEEP OUT OF REACH OF CHILDREN.
WARNINGS SECTION
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.
OTC - QUESTIONS SECTION
Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
shopuriel.com
Lot:
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-1397-1 | Aurum Hypericum | 10 in 1 BOX | LIQUID | 10 | 1 | |
| 48951-1397-1 | Aurum Hypericum | 10 mL in 1 AMPULE | LIQUID | 10 | 1 |
Products#
Every source-derived product name is available through these pages.
- Aurum Hypericum
- MAGNESIUM HYDROXIDE
- MAGNESIUM CATION
- ROYAL JELLY
- SILICON DIOXIDE
- LACTOSE
- PHOSPHORIC ACID
- STRYCHNOS IGNATII SEED
- GOLD TRICHLORIDE
- GOLD CATION (3+)
- ST. JOHN'S WORT
- SODIUM CHLORIDE
- AVENA SATIVA FLOWERING TOP
- ORYCTOLAGUS CUNICULUS LIVER
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-1397 | 48951-1397-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| MAGNESIUM HYDROXIDE | NBZ3QY004S | ACTIB |
| ROYAL JELLY | L497I37F0C | ACTIB |
| SILICON DIOXIDE | ETJ7Z6XBU4 | ACTIB |
| LACTOSE | J2B2A4N98G | IACT |
| PHOSPHORIC ACID | E4GA8884NN | ACTIB |
| STRYCHNOS IGNATII SEED | 1NM3M2487K | ACTIB |
| GOLD TRICHLORIDE | 15443PR153 | ACTIB |
| ST. JOHN'S WORT | UFH8805FKA | ACTIB |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| AVENA SATIVA FLOWERING TOP | MA9CQJ3F7F | ACTIB |
| ORYCTOLAGUS CUNICULUS LIVER | 7A99K6361Z | ACTIB |
| WATER | 059QF0KO0R | IACT |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Aurum Hypericum | AURUM HYPERICUM | Uriel Pharmacy, Inc | 2df4f968-af1d-82f1-e063-6294a90a65be | 2025-02-12 | Warnings | 48951-1397-1 48951-1397 48951139701 2df4f968-af1e-82f1-e063-6294a90a65be 2df4f968-af1d-82f1-e063-6294a90a65be |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
