Prunus Iron Special Order
- Manufacturer
- Uriel Pharmacy Inc.
- Effective date
- 2018-05-09
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:10:19
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: Prunus spinosa e flor. et summ. 6X, Hematite 6X
INACTIVE INGREDIENT SECTION
Inactive Ingredient: Distilled water
OTC - PURPOSE SECTION
Use: Temporary relief of fatigue.
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.
REFRIGERATE AFTER OPENING.
BEST WHEN USED WITHIN 90 DAYS OF OPENING.
OTC - QUESTIONS SECTION
Questions? Call 866.642.2858
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 |
|---|---|---|---|---|---|---|
| 48951-8333-3 | Prunus Iron Special Order | 60 mL in 1 BOTTLE, DROPPER | LIQUID | 60 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-8333 | PRUNUS IRON SPECIAL ORDER LIQUID [URIEL PHARMACY INC.] | 1 | Legacy NDC, 1 package rows | 20180614_6bcb40e7-426c-058e-e053-2991aa0ad7c7.zip |
Products#
Every source-derived product name is available through these pages.
- Prunus Iron Special Order
- WATER
- FERRIC OXIDE RED
- PRUNUS SPINOSA FLOWER BUD
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-8333 | 48951-8333-3 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| FERRIC OXIDE RED | 1K09F3G675 | ACTIB |
| PRUNUS SPINOSA FLOWER BUD | 53Y84VPS2W | 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 |
|---|---|---|---|---|---|---|
| 6bcb40e7-426d-058e-e053-2991aa0ad7c7 | 6bcb40e7-426c-058e-e053-2991aa0ad7c7 | 2018-05-09 | Warnings | 6bcb40e7-426d-058e-e053-2991aa0ad7c7 6bcb40e7-426c-058e-e053-2991aa0ad7c7 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
