Bryophyllum Argento 3X
- Manufacturer
- Uriel Pharmacy. Inc
- Effective date
- 2024-12-20
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 20:44:38
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: Bryophyllum (Life plant)3X, Argento cultum (Vegetabilized silver) 3X
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Distilled water, 20% Organic cane alcohol
Prepared using rhythmical processes.
OTC - PURPOSE SECTION
Use: Temporary relief of sleeplessness.
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. 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 Lot:
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 48951-2158-3 | 2026-01-29 | C162847 | 48780-1 | 49896155-a31c-586f-e063-e6dba90add90 | Bryophyllum Argento 3X |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-2158 | BRYOPHYLLUM ARGENTO 3X LIQUID [URIEL PHARMACY. INC] | 1 | Unmatched | 20241222_29ba4e19-11d2-b7fb-e063-6394a90a9faf.zip |
Products#
Every source-derived product name is available through these pages.
- Bryophyllum Argento 3X
- KALANCHOE DAIGREMONTIANA LEAF
- WATER
- ALCOHOL
- SILVER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-2158 | 48951-2158-3 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| KALANCHOE DAIGREMONTIANA LEAF | L6X13JKL8O | ACTIB |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| SILVER | 3M4G523W1G | 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 |
|---|---|---|---|---|---|---|
| 4d7a9183-2bb2-99cd-e063-6394a90af666 | 29ba4e19-11d2-b7fb-e063-6394a90a9faf | 2026-03-20 | Warnings | 29ba4e19-11d2-b7fb-e063-6394a90a9faf |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
