Berberis Prunus
- Manufacturer
- Uriel Pharmacy Inc.
- Effective date
- 2024-03-06
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 02:26:17
Label at a glance#
ProductBerberis Prunus
Active ingredientECHINACEA ANGUSTIFOLIA, SILVER, BERBERIS VULGARIS FRUIT, BOS TAURUS NASAL MUCOSA, SILICON DIOXIDE, SLOE, FERROSOFERRIC PHOSPHATE
Label structure9 sections
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: Berberis (Barberry) 2X, Echinacea (Purple coneflower) 2X, Prunus spinosa (Blackthorn) 2X, Vivianite (Nat. ferrous phosphate) 6X, Argentum met. (Silver) 8X, Tunica mucosa nasi (Bovine nasal mucosa) 8X, Quartz (Rock crystal) 30X
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Distilled water, 20% Organic cane alcohol, Lactose
"prepared using rhythmical processes"
OTC - PURPOSE SECTION
Use: Temporary relief of nasal congestion.
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 lactose. 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
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-2140-3 | Berberis Prunus | 60 mL in 1 BOTTLE, DROPPER | LIQUID | 60 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-2140 | BERBERIS PRUNUS LIQUID [URIEL PHARMACY INC.] | 2 | Legacy NDC, 1 package rows | 20240308_c3df8739-02db-0134-e053-2a95a90abe26.zip |
Products#
Every source-derived product name is available through these pages.
- Berberis Prunus
- ECHINACEA ANGUSTIFOLIA
- SILVER
- WATER
- LACTOSE, UNSPECIFIED FORM
- BERBERIS VULGARIS FRUIT
- BOS TAURUS NASAL MUCOSA
- SILICON DIOXIDE
- ALCOHOL
- SLOE
- FERROSOFERRIC PHOSPHATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-2140 | 48951-2140-3 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ECHINACEA ANGUSTIFOLIA | VB06AV5US8 | ACTIB |
| SILVER | 3M4G523W1G | ACTIB |
| WATER | 059QF0KO0R | IACT |
| LACTOSE, UNSPECIFIED FORM | J2B2A4N98G | IACT |
| BERBERIS VULGARIS FRUIT | 6XEF22AHC3 | ACTIB |
| BOS TAURUS NASAL MUCOSA | 343455G79K | ACTIB |
| SILICON DIOXIDE | ETJ7Z6XBU4 | ACTIB |
| ALCOHOL | 3K9958V90M | IACT |
| SLOE | 3MLB4858X7 | ACTIB |
| FERROSOFERRIC PHOSPHATE | 91GQH8I5F7 | 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 |
|---|---|---|---|---|---|---|
| 12ffbba5-0539-3dc3-e063-6394a90aa972 | c3df8739-02db-0134-e053-2a95a90abe26 | 2024-03-06 | Warnings | 12ffbba5-0539-3dc3-e063-6394a90aa972 c3df8739-02db-0134-e053-2a95a90abe26 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.