FDA.reportPublic FDA data

Disci Viscum Comp.cum Stanno DKS Special Order

Manufacturer
Uriel Pharmacy Inc.
Effective date
2018-09-10
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 00:49:49

Label at a glance#

ProductDisci Viscum Comp.cum Stanno DKS Special Order
Active ingredientFORMICA RUFA, URTICA DIOICA, VESPA CRABRO, COPPER, BAMBUSA VULGARIS WHOLE, BOS TAURUS INTERVERTEBRAL DISC, EQUISETUM ARVENSE TOP, TIN, VISCUM ALBUM FRUITING TOP
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR TOPICAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Formica (Red wood ant) 3X/12X/30X, Urtica dioica (Stinging nettle) 3X/20X, Vespa crabro (Hornet) 6X/20X, Cuprum met. (Copper) 8X, Bambusa (Bamboo) 12X, Disci intervert. (Bovine intervertebral discs of the cervical, thoracic and lumbar spine) 12X, Equisetum (Common horsetail) 12X, Stannum met. (Metallic tin) 12X, Viscum Mali (Apple tree mistletoe) 12X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Organic olive oil, Lanolin, Beeswax, Lanolin alcohol, Tea Tree Oil, Grapefruit seed extract

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. 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

Disci Viscum Comp. cum Stanno DKS Special OrderDisci Viscum Comp. cum Stanno DKS Special Order

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-415048951-4150-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
OLIVE OIL6UYK2W1W1EIACT
LANOLIN7EV65EAW6HIACT
YELLOW WAX2ZA36H0S2VIACT
LANOLIN ALCOHOLS884C3FA9HEIACT
CITRUS PARADISI SEED12F08874Y7IACT
FORMICA RUFA55H0W83JO5ACTIB
URTICA DIOICA710FLW4U46ACTIB
VESPA CRABROK3ALM8S49HACTIB
COPPER789U1901C5ACTIB
BAMBUSA VULGARIS WHOLEWCD45M1BSKACTIB
BOS TAURUS INTERVERTEBRAL DISC0A04Z76C13ACTIB
EQUISETUM ARVENSE TOP1DP6Y6B65ZACTIB
TIN387GMG9FH5ACTIB
VISCUM ALBUM FRUITING TOPBK9092J5MPACTIB
TEA TREE OILVIF565UC2GIACT

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
0e9c5d61-346d-e95f-e063-6294a90a2b43b3bedea7-a2e9-4bcf-86fc-13f2c8e37be52024-01-10WarningsExact identifier
spl set id: b3bedea7-a2e9-4bcf-86fc-13f2c8e37be5

Reported adverse events (FAERS/openFDA)#

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