Arnica Echinacea
- Manufacturer
- Uriel Pharmacy Inc
- Effective date
- 2024-12-02
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:29:18
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
INDICATIONS & USAGE SECTION
Directions: FOR ORAL USE ONLY.
DOSAGE & ADMINISTRATION SECTION
Dissolve pellets under the tongue 3-4 times daily. Ages 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: Consult a doctor.
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients: Bellis per. (Daisy) 5X, Echinacea (Purple coneflower) 5X, Hamamelis (Witch hazel) 5X, Hypericum (St. John’s Wort) 5X, Achillea (Yarrow) 6X, Aconitum (Monkshood) 6X, Arnica 6X, Atropa belladonna (Nightshade) 6X, Calendula 6X, Chamomilla (Chamomile) 6X, Hepar sulfuris (Liver of lime) 9X, Mercurius solubilis (Mercury amidonitrate) 9X, Symphytum (Comfrey) 9X
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Organic sucrose
Prepared using rhythmical processes.
OTC - PURPOSE SECTION
Uses: Temporary relief of bruises, sprains and minor cuts.
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. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. Do not use if allergic to any ingredient. Contains traces of 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
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 |
|---|---|---|---|---|---|---|
| 48951-1381-2 | Arnica Echinacea | 1350 in 1 BOTTLE, GLASS | PELLET | 1350 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-1381 | ARNICA ECHINACEA PELLET [URIEL PHARMACY INC] | 1 | 1 package rows | 20241207_2873a6cf-8a95-e226-e063-6394a90a27f0.zip |
Products#
Every source-derived product name is available through these pages.
- Arnica Echinacea
- SUCROSE
- BELLIS PERENNIS
- ECHINACEA, UNSPECIFIED
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK
- ST. JOHN'S WORT
- ACHILLEA MILLEFOLIUM
- ACONITUM NAPELLUS
- ARNICA MONTANA
- ATROPA BELLADONNA
- CALENDULA OFFICINALIS FLOWERING TOP
- MATRICARIA RECUTITA
- CALCIUM SULFIDE
- MERCURIUS SOLUBILIS
- COMFREY ROOT
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-1381 | 48951-1381-2 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SUCROSE | C151H8M554 | IACT |
| BELLIS PERENNIS | 2HU33I03UY | ACTIB |
| ECHINACEA, UNSPECIFIED | 4N9P6CC1DX | ACTIB |
| HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK | T7S323PKJS | ACTIB |
| ST. JOHN'S WORT | UFH8805FKA | ACTIB |
| ACHILLEA MILLEFOLIUM | 2FXJ6SW4PK | ACTIB |
| ACONITUM NAPELLUS | U0NQ8555JD | ACTIB |
| ARNICA MONTANA | O80TY208ZW | ACTIB |
| ATROPA BELLADONNA | WQZ3G9PF0H | ACTIB |
| CALENDULA OFFICINALIS FLOWERING TOP | 18E7415PXQ | ACTIB |
| MATRICARIA RECUTITA | G0R4UBI2ZZ | ACTIB |
| CALCIUM SULFIDE | 1MBW07J51Q | ACTIB |
| MERCURIUS SOLUBILIS | 324Y4038G2 | ACTIB |
| COMFREY ROOT | M9VVZ08EKQ | 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 |
|---|---|---|---|---|---|---|
| 28739b39-b95c-dfa6-e063-6394a90aa006 | 2873a6cf-8a95-e226-e063-6394a90a27f0 | 2024-12-02 | Warnings | 28739b39-b95c-dfa6-e063-6394a90aa006 2873a6cf-8a95-e226-e063-6394a90a27f0 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
