Ferrum Silicicum Urtica
- Manufacturer
- Uriel Pharmacy Inc. | Uriel Pharmacy, Inc.
- Effective date
- 2025-01-07
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 8
- Source
- full-release
- Hydrated at
- 2026-06-01 02:30:06
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 Ingredient: Anisum (Anise) 1X, Urtica dioica (Stinging nettle) 3X, Ferrum sesquioxide (Iron oxide) 6X, Nontronite - Ferrum silic. (Nat. Iron silicate) 6X
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Water, Salt, Lactose
Prepared using rhythmical processes.
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 homepoathic 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 |
|---|---|---|---|---|---|---|
| 48951-4176-1 | Ferrum Silicicum Urtica | 10 in 1 BOX | LIQUID | 10 | 8 | |
| 48951-4176-1 | Ferrum Silicicum Urtica | 1 mL in 1 AMPULE | LIQUID | 1 | 8 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-4176 | FERRUM SILICICUM URTICA LIQUID [URIEL PHARMACY INC.] | 8 | Current NDC, 2 package rows | 20250109_09829ac4-c074-7315-e063-6394a90adf59.zip |
Products#
Every source-derived product name is available through these pages.
- Ferrum Silicicum Urtica
- ANISE
- SODIUM CHLORIDE
- URTICA DIOICA
- SILICON DIOXIDE
- FERRIC OXIDE RED
- WATER
- LACTOSE, UNSPECIFIED FORM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-4176 | 48951-4176-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ANISE | 21C2F5E8RE | ACTIB |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| URTICA DIOICA | 710FLW4U46 | ACTIB |
| SILICON DIOXIDE | ETJ7Z6XBU4 | ACTIB |
| FERRIC OXIDE RED | 1K09F3G675 | ACTIB |
| WATER | 059QF0KO0R | IACT |
| LACTOSE, UNSPECIFIED FORM | J2B2A4N98G | 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 |
|---|---|---|---|---|---|---|
| Ferrum Silicicum Urtica | FERRUM SILICICUM URTICA | Uriel Pharmacy Inc. | 09829ac4-c074-7315-e063-6394a90adf59 | 2025-01-07 | Warnings | 48951-4176-1 48951-4176 48951417601 2b25a031-6146-c44c-e063-6394a90ab6ff 09829ac4-c074-7315-e063-6394a90adf59 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
