Arnica Forte
- Manufacturer
- Uriel Pharmacy Inc.
- Effective date
- 2018-10-11
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:10:27
Label at a glance#
ProductArnica Forte
Active ingredientARNICA MONTANA FLOWER
Label structure9 sections
Contacts and useful links#
Websitewww.urielpharmacy.com
www.urielpharmacy.com
www.urielpharmacy.comLabel contents#
Full prescribing information#
INDICATIONS & USAGE SECTION
Directions: FOR TOPICAL USE ONLY.
DOSAGE & ADMINISTRATION SECTION
Apply to skin as needed. Under age 2: Consult a doctor.
OTC - ACTIVE INGREDIENT SECTION
Active Ingredient: 100 gm contains: 20 gm Arnica 1X
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Distilled water, Organic cane alcohol, Glycerin, Sodium alginate, Lavender oil, Sorbic acid, Tea tree oil, Grapefruit seed extract
OTC - PURPOSE SECTION
Uses: Temporary relief of bruises, sprains and/or minor cuts.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
KEEP OUT OF REACH OF CHILDREN.
WARNINGS SECTION
Warnings: FOR EXTERNAL USE ONLY
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, if conditions worsen or persist or accidental ingestion occurs. If pregnant or nursing consult a doctor before use. Avoid contact with eyes. 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
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 48951-1308-5 | 2026-01-29 | C162847 | 48780-1 | 49896155-aa4d-586f-e063-e6dba90add90 | Arnica Forte |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-1308-5 | Arnica Forte | 60 g in 1 TUBE | GEL | 60 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-1308 | ARNICA FORTE GEL [URIEL PHARMACY INC.] | 1 | Legacy NDC, 1 package rows | 20181012_77f72303-08a6-a101-e053-2991aa0a62eb.zip |
Products#
Every source-derived product name is available through these pages.
- Arnica Forte
- SORBIC ACID
- SODIUM ALGINATE
- CITRUS PARADISI SEED
- ARNICA MONTANA FLOWER
- WATER
- ALCOHOL
- GLYCERIN
- LAVENDER OIL
- TEA TREE OIL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-1308 | 48951-1308-5 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SORBIC ACID | X045WJ989B | IACT |
| SODIUM ALGINATE | C269C4G2ZQ | IACT |
| CITRUS PARADISI SEED | 12F08874Y7 | IACT |
| ARNICA MONTANA FLOWER | OZ0E5Y15PZ | ACTIB |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| LAVENDER OIL | ZBP1YXW0H8 | IACT |
| TEA TREE OIL | VIF565UC2G | 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 |
|---|---|---|---|---|---|---|
| 77f72303-08a7-a101-e053-2991aa0a62eb | 77f72303-08a6-a101-e053-2991aa0a62eb | 2018-10-11 | Warnings | 77f72303-08a7-a101-e053-2991aa0a62eb 77f72303-08a6-a101-e053-2991aa0a62eb |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.