Cartilago Argentum
- Manufacturer
- Uriel Pharmacy Inc.
- Effective date
- 2024-11-26
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 02:29:05
Label at a glance#
ProductCartilago Argentum
Active ingredientSILVER, MANDRAGORA OFFICINARUM ROOT, ACONITUM NAPELLUS, ANTIMONY TRISULFIDE, ARNICA MONTANA, BETULA PUBESCENS LEAF, BOS TAURUS CARTILAGE
Label structure9 sections
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: Mandragora (Mandrake) 5X, Aconitum (Monkshood) 6X, Antimonite (Nat. antimony trisulfide) 6X, Arnica 6X, Betula (Silver birch leaves) 6X, Argentum met. (Silver) 8X, Cartilago articularis (Bovine cartilage - hip joint/knee joint) 8X
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Water, Salt, Lactose
Prepared using rhythmical processes.
OTC - PURPOSE SECTION
Use: Temporary relief of aches and pains in the joints.
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
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-3261-1 | Cartilago Argentum | 1 mL in 1 AMPULE | LIQUID | 1 | 2 | |
| 48951-3261-1 | Cartilago Argentum | 10 in 1 BOX | LIQUID | 10 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-3261 | CARTILAGO ARGENTUM LIQUID [URIEL PHARMACY INC.] | 2 | 2 package rows | 20241127_0f3cbba8-a329-ae4f-e063-6294a90a4cab.zip |
Products#
Every source-derived product name is available through these pages.
- Cartilago Argentum
- SILVER
- WATER
- SODIUM CHLORIDE
- LACTOSE
- MANDRAGORA OFFICINARUM ROOT
- ACONITUM NAPELLUS
- ANTIMONY TRISULFIDE
- ARNICA MONTANA
- BETULA PUBESCENS LEAF
- BOS TAURUS CARTILAGE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-3261 | 48951-3261-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SILVER | 3M4G523W1G | ACTIB |
| WATER | 059QF0KO0R | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| LACTOSE | J2B2A4N98G | IACT |
| MANDRAGORA OFFICINARUM ROOT | I2XCB174VB | ACTIB |
| ACONITUM NAPELLUS | U0NQ8555JD | ACTIB |
| ANTIMONY TRISULFIDE | F79059A38U | ACTIB |
| ARNICA MONTANA | O80TY208ZW | ACTIB |
| BETULA PUBESCENS LEAF | 84SOH0O3OO | ACTIB |
| BOS TAURUS CARTILAGE | UE77B10IIY | 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 |
|---|---|---|---|---|---|---|
| 27d56406-22c7-c2db-e063-6394a90a2871 | 0f3cbba8-a329-ae4f-e063-6294a90a4cab | 2024-11-26 | Warnings | 27d56406-22c7-c2db-e063-6394a90a2871 0f3cbba8-a329-ae4f-e063-6294a90a4cab |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.