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#

ProductAurum Hypericum
Active ingredientMAGNESIUM HYDROXIDE, ROYAL JELLY, SILICON DIOXIDE, PHOSPHORIC ACID, STRYCHNOS IGNATII SEED, GOLD TRICHLORIDE, ST. JOHN'S WORT, AVENA SATIVA FLOWERING TOP, ORYCTOLAGUS CUNICULUS LIVER
Label structure9 sections

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

Aurum Hypericum AmpulesAurum Hypericum Ampules

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6e3c022f-0786-43f1-8857-edff89d5153fProduct name120260309
95250459-30e4-45c1-b08a-993044f49109Product name220250805
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362d7abb-94e6-4c60-9a58-266894157713Product name120231023
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6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
2641ccb3-721d-4fbf-9f2f-ca2f18157a62Product name320210309
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
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c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1397-1Aurum Hypericum10 in 1 BOXLIQUID101
48951-1397-1Aurum Hypericum10 mL in 1 AMPULELIQUID101

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-139748951-1397-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Aurum HypericumAURUM HYPERICUMUriel Pharmacy, Inc2df4f968-af1d-82f1-e063-6294a90a65be2025-02-12WarningsExact identifier
ndc (package): 48951-1397-1
ndc (product): 48951-1397
ndc11 (package): 48951139701
spl id: 2df4f968-af1e-82f1-e063-6294a90a65be
spl set id: 2df4f968-af1d-82f1-e063-6294a90a65be

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.