FDA.reportPublic FDA data

Arnica Nettle

Manufacturer
Uriel Pharmacy Inc.
Effective date
2022-01-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:11:32

Label at a glance#

ProductArnica Nettle
Active ingredientARNICA MONTANA FLOWER, CALENDULA OFFICINALIS FLOWERING TOP, COMFREY ROOT, THUJA OCCIDENTALIS WHOLE, URTICA URENS, LARIX DECIDUA RESIN, LYTTA VESICATORIA, SILVER
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR TOPICAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Apply gel to skin as soon as possible. Reapply several times daily. 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 e summ. (American arborvitae) 2X, Symphytum (Comfrey) 2X, Cantharis (Spanish fly) 7X, Colloidal silver 8X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled water, Glycerin, Organic cane alcohol, Sodium alginate, Aloe vera, Cajeput oil, Rosemary oil, Sorbic acid, Tea tree oil, Thyme oil, Grapefruit seed extract

OTC - PURPOSE SECTION

Uses: Temporary relief of burns, sunburn, insect bites, bee stings and rashes.

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.
FOR BURNS, SEEK MEDICAL ATTENTION IF NEEDED.

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

Arnica Nettle GelArnica Nettle Gel

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-131548951-1315-5

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM ALGINATEC269C4G2ZQIACT
SORBIC ACIDX045WJ989BIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
ALOE VERA LEAFZY81Z83H0XIACT
CAJUPUT OILJ3TO6BUQ37IACT
ROSEMARY OIL8LGU7VM393IACT
TEA TREE OILVIF565UC2GIACT
THYME OIL2UK410MY6BIACT
CITRUS PARADISI SEED12F08874Y7IACT
ARNICA MONTANA FLOWEROZ0E5Y15PZACTIB
CALENDULA OFFICINALIS FLOWERING TOP18E7415PXQACTIB
COMFREY ROOTM9VVZ08EKQACTIB
THUJA OCCIDENTALIS WHOLE5HBV6WCE3NACTIB
URTICA URENSIHN2NQ5OF9ACTIB
LARIX DECIDUA RESINAD8LJ73GQFACTIB
LYTTA VESICATORIA3Q034RO3BTACTIB
SILVER3M4G523W1GACTIB

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d67ec807-89bd-854a-e053-2a95a90a65a681b45dc4-40f6-7236-e053-2a91aa0ad4df2022-01-26WarningsExact identifier
spl id: d67ec807-89bd-854a-e053-2a95a90a65a6
spl set id: 81b45dc4-40f6-7236-e053-2a91aa0ad4df

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.