Cartilago Argentum
- Manufacturer
- Uriel Pharmacy Inc.
- Effective date
- 2025-11-18
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- full-release
- Hydrated at
- 2026-06-01 02:35:13
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
INDICATIONS & USAGE SECTION
Directions:FOR TOPICAL USE ONLY.
DOSAGE & ADMINISTRATION SECTION
Apply to joint(s) several times daily or as needed. Under age 2: Consult a doctor.
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients: Betula (Silver birch leaves) 3X, Mandragora off. (Mandrake) 3X, Antimonite (Nat. antimony trisulfide) 5X, Aconitum (Monkshood) 6X, Arnica 6X, Argentum met. (Silver) 8X, Cartilago articularis (Bovine cartilage - knee joint) 8X
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Spring water, Stearic acid, Isopropyl myristate, Lavender oil, Cetyl alcohol, Polyoxyl 40 stearate, Stearyl alcohol, Xanthan gum, Distilled water, Sorbic acid, Tea tree oil, Frankincense oil, Grapefruit seed extract, Myrrh oil, Lactose
Prepared using rhythmical processes.
OTC - PURPOSE SECTION
Use: Temporary relief of joint pain.
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, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. Contains traces of lactose. 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 Lot:
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-3260-5 | Cartilago Argentum | 60 g in 1 TUBE | CREAM | 60 | 4 |
Products#
Every source-derived product name is available through these pages.
- Cartilago Argentum
- ISOPROPYL MYRISTATE
- ACONITUM NAPELLUS
- ARNICA MONTANA
- SILVER
- STEARIC ACID
- FRANKINCENSE OIL
- BOS TAURUS CARTILAGE
- WATER
- SORBIC ACID
- MYRRH OIL
- BETULA PUBESCENS LEAF
- ANTIMONY TRISULFIDE
- LAVENDER OIL
- CETYL ALCOHOL
- POLYOXYL 40 STEARATE
- STEARYL ALCOHOL
- XANTHAN GUM
- TEA TREE OIL
- CITRUS PARADISI SEED
- LACTOSE, UNSPECIFIED FORM
- MANDRAGORA OFFICINARUM ROOT
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-3260 | 48951-3260-5 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| Cartilago Argentum | CARTILAGO ARGENTUM | Uriel Pharmacy Inc. | 0f3bf8ce-0a60-4a79-e063-6294a90a3932 | 2025-11-18 | Warnings | 48951-3260-5 48951-3260 48951326005 43e57be5-d1f4-b1c8-e063-6394a90ac681 0f3bf8ce-0a60-4a79-e063-6294a90a3932 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
