FDA.reportPublic FDA data

Graphite Belladonna Special Order

Manufacturer
Uriel Pharmacy Inc.
Effective date
2018-05-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:57:39

Label at a glance#

ProductGraphite Belladonna Special Order
Active ingredientBOS TAURUS BRAIN, TIN, GRAPHITE, HELLEBORUS FOETIDUS ROOT, SILVER SULFIDE, ATROPA BELLADONNA, AMANITA MUSCARIA FRUITING BODY
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE.

DOSAGE & ADMINISTRATION SECTION

Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Helleborus niger e pl.
tota 4X, Agaricus e pl. tota 6X, Argentite
6X, Regio substantia nigra 6X, Stannum metallicum 20X, Atropa belladonna e rad. 30X, Graphite 30X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Salt, 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: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Contains traces of lactose. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult
a doctor before use.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GraphiteBelladonnaSpecialOrderAmpulesGraphiteBelladonnaSpecialOrderAmpules

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-510748951-5107-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
BOS TAURUS BRAINA1YEE2DB8ZACTIB
TIN387GMG9FH5ACTIB
GRAPHITE4QQN74LH4OACTIB
HELLEBORUS FOETIDUS ROOT332Y7EES96ACTIB
SILVER SULFIDE9ZB10YHC1CACTIB
ATROPA BELLADONNAWQZ3G9PF0HACTIB
WATER059QF0KO0RIACT
SODIUM CHLORIDE451W47IQ8XIACT
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT
AMANITA MUSCARIA FRUITING BODYDIF093I037ACTIB

Source Document#

Source XML · Source PDF

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
cf336778-6cf9-5fbc-e053-2995a90ad2776cbd257b-4e14-c6cf-e053-2991aa0ab4262021-10-25WarningsExact identifier
spl set id: 6cbd257b-4e14-c6cf-e053-2991aa0ab426

Reported adverse events (FAERS/openFDA)#

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