Aurum Hypericum
- Manufacturer
- Uriel Pharmacy Inc.
- Effective date
- 2025-08-19
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- full-release
- Hydrated at
- 2026-06-01 02:34:51
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
INDICATIONS & USAGE SECTION
Directions: FOR ORAL USE ONLY.
DOSAGE & ADMINISTRATION SECTION
Take 3-4 times daily. Ages 12 and older: 10 drops.
Ages 2-11: 5 drops. Under age 2: Consult a doctor.
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. (Orthosphoric acid) 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
"prepared using rhythmical processes"
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Distilled water, 20% Organic cane alcohol, Lactose
OTC - PURPOSE SECTION
Use: Temporary relief of headache.
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. 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.
OTC - QUESTIONS SECTION
Questions? Call 866.642.2858
Made with care by Uriel, East Troy, WI 53120
shopuriel.com
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-1368-3 | Aurum Hypericum | 60 mL in 1 BOTTLE, DROPPER | LIQUID | 60 | 4 |
Products#
Every source-derived product name is available through these pages.
- Aurum Hypericum
- MAGNESIUM HYDROXIDE
- MAGNESIUM CATION
- STRYCHNOS IGNATII SEED
- ROYAL JELLY
- WATER
- ALCOHOL
- AVENA SATIVA FLOWERING TOP
- PHOSPHORIC ACID
- SILICON DIOXIDE
- GOLD TRICHLORIDE
- GOLD CATION (3+)
- ST. JOHN'S WORT
- LACTOSE, UNSPECIFIED FORM
- ANHYDROUS LACTOSE
- MAMMAL LIVER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-1368 | 48951-1368-3 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| MAGNESIUM HYDROXIDE | NBZ3QY004S | ACTIB |
| STRYCHNOS IGNATII SEED | 1NM3M2487K | ACTIB |
| ROYAL JELLY | L497I37F0C | ACTIB |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| AVENA SATIVA FLOWERING TOP | MA9CQJ3F7F | ACTIB |
| PHOSPHORIC ACID | E4GA8884NN | ACTIB |
| SILICON DIOXIDE | ETJ7Z6XBU4 | ACTIB |
| GOLD TRICHLORIDE | 15443PR153 | ACTIB |
| ST. JOHN'S WORT | UFH8805FKA | ACTIB |
| LACTOSE, UNSPECIFIED FORM | J2B2A4N98G | IACT |
| MAMMAL LIVER | D0846624BI | ACTIB |
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. | 0c3ed6fe-8dce-0496-e063-6394a90add56 | 2025-08-19 | Warnings | 48951-1368-3 48951-1368 48951136803 3cbd7956-f62d-5668-e063-6294a90a3de3 0c3ed6fe-8dce-0496-e063-6394a90add56 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
