Arnica Bryonia Special Order
- Manufacturer
- Uriel Pharmacy Inc.
- Effective date
- 2018-05-02
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:09:42
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. Age 12 and older: 10 drops.
Ages 2-11: 5 drops. Under age 2: Consult a doctor.
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients: Arnica 2X, Bryonia (White bryony) 3X, Aconitum (Monkshood) 4X
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Distilled water, 20% Organic cane alcohol
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 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 you are 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
www.urielpharmacy.com
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-1288-3 | Arnica Bryonia Special Order | 60 mL in 1 BOTTLE, DROPPER | LIQUID | 60 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-1288 | ARNICA BRYONIA SPECIAL ORDER LIQUID [URIEL PHARMACY INC.] | 1 | Legacy NDC, 1 package rows | 20180515_6b3ec25a-65bb-de80-e053-2991aa0aa70d.zip |
Products#
Every source-derived product name is available through these pages.
- Arnica Bryonia Special Order
- ARNICA MONTANA
- BRYONIA ALBA ROOT
- ACONITUM NAPELLUS
- WATER
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-1288 | 48951-1288-3 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ARNICA MONTANA | O80TY208ZW | ACTIB |
| BRYONIA ALBA ROOT | T7J046YI2B | ACTIB |
| ACONITUM NAPELLUS | U0NQ8555JD | ACTIB |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | 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 |
|---|---|---|---|---|---|---|
| 6b3ec25a-65bc-de80-e053-2991aa0aa70d | 6b3ec25a-65bb-de80-e053-2991aa0aa70d | 2018-05-02 | Warnings | 6b3ec25a-65bc-de80-e053-2991aa0aa70d 6b3ec25a-65bb-de80-e053-2991aa0aa70d |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
