FDA.reportPublic FDA data

Arnica Hypericum DKS Special Order

Manufacturer
Uriel Pharmacy Inc.
Effective date
2019-06-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:04:25

Label at a glance#

ProductArnica Hypericum DKS Special Order
Active ingredientACONITUM NAPELLUS, URTICA DIOICA, ST. JOHN'S WORT, GOLD, OXALIS STRICTA WHOLE, SEDUM ROSEUM WHOLE, ARNICA MONTANA FLOWER, PENOXSULAM, ANTIMONY
Label structure9 sections

Label 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 Ingredients: Hypericum (St. John’s Wort) 5X/10X, Aconitum (Monkshood) 6X, Aurum met. (Metallic gold) 6X, Oxalis (Wood sorrel) 6X, Stibium met. (Antimony) 6X, Urtica dioica (Stinging nettle) 6X, Arnica 6X/12X, Granite (Primitive rock containing quartz, feldspar, mica) 12X, Rosa (Garden rose) 6X/15X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Organic olive oil, Lanolin, Beeswax, Distilled water, Sunflower seed oil, Tea tree oil, Grapefruit seed extract, Lactose

OTC - PURPOSE SECTION

Use: Temporary relief of headache.

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. Contains traces of lactose. 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

Arnica Hypericum DKS Special Order OintmentArnica Hypericum DKS Special Order Ointment

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
48951-130448951-1304-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACONITUM NAPELLUSU0NQ8555JDACTIB
URTICA DIOICA710FLW4U46ACTIB
ST. JOHN'S WORTUFH8805FKAACTIB
GOLD79Y1949PYOACTIB
OXALIS STRICTA WHOLE3STW243384ACTIB
SEDUM ROSEUM WHOLERH0WP583U3ACTIB
OLIVE OIL6UYK2W1W1EIACT
YELLOW WAX2ZA36H0S2VIACT
WATER059QF0KO0RIACT
CITRUS PARADISI SEED12F08874Y7IACT
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZACTIB
PENOXSULAM784ELC1SCZACTIB
ANTIMONY9IT35J3UV3ACTIB
SUNFLOWER OIL3W1JG795YIIACT
TEA TREE OILVIF565UC2GIACT
LANOLIN7EV65EAW6HIACT
SORBIC ACIDX045WJ989BIACT

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
c8c1dc91-db22-f7da-e053-2a95a90a43286e72d4d0-41a3-28ff-e053-2991aa0a2de52021-08-04WarningsExact identifier
spl set id: 6e72d4d0-41a3-28ff-e053-2991aa0a2de5

Reported adverse events (FAERS/openFDA)#

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