Arnica Nettle Burn and Bite
- Manufacturer
- Uriel Pharmacy Inc.
- Effective date
- 2018-04-17
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 00:59:54
Label at a glance#
ProductArnica Nettle Burn and Bite
Active ingredientURTICA URENS, ARNICA MONTANA FLOWER, CALENDULA OFFICINALIS FLOWERING TOP, LARIX DECIDUA RESIN, THUJA OCCIDENTALIS WHOLE, COMFREY ROOT, LYTTA VESICATORIA, SILVER
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
Use up to every hour. Ages 2 and older: 1-2 sprays. Under age 2: Consult a doctor.
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients: 100 gm contains: 4.5 gm Urtica urens (Small nettle) 1X, 1.5 gm Arnica 1X; Calendula 2X, Resina laricis (Larch resin) 2X, Thuja (American arborvitae) 2X, Symphytum (Comfrey) 2X, Cantharis (Spanish fly) 7X, Colloidal silver 8X
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Distilled water, Organic cane alcohol
OTC - PURPOSE SECTION
Uses: Temporary relief of minor burns and insect bites.
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 seals on box are broken or missing.
FOR BURNS, SEEK MEDICAL ATTENTION IF NEEDED.
OTC - QUESTIONS SECTION
Questions? Call 866.642.2858 Uriel, East Troy, WI 53120 www.urielpharmacy.com
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Products#
Every source-derived product name is available through these pages.
- Arnica Nettle Burn and Bite
- WATER
- ALCOHOL
- URTICA URENS
- ARNICA MONTANA FLOWER
- CALENDULA OFFICINALIS FLOWERING TOP
- LARIX DECIDUA RESIN
- THUJA OCCIDENTALIS WHOLE
- COMFREY ROOT
- LYTTA VESICATORIA
- SILVER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-1282 | 48951-1282-2 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| URTICA URENS | IHN2NQ5OF9 | ACTIB |
| ARNICA MONTANA FLOWER | OZ0E5Y15PZ | ACTIB |
| CALENDULA OFFICINALIS FLOWERING TOP | 18E7415PXQ | ACTIB |
| LARIX DECIDUA RESIN | AD8LJ73GQF | ACTIB |
| THUJA OCCIDENTALIS WHOLE | 5HBV6WCE3N | ACTIB |
| COMFREY ROOT | M9VVZ08EKQ | ACTIB |
| LYTTA VESICATORIA | 3Q034RO3BT | ACTIB |
| SILVER | 3M4G523W1G | 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 |
|---|---|---|---|---|---|---|
| 13909074-eeb2-c1ff-e063-6394a90ac7f0 | e8d31bdf-4e7b-4524-8639-acc68195e28e | 2024-03-13 | Warnings | e8d31bdf-4e7b-4524-8639-acc68195e28e |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.