Robinia Nicotiana

Manufacturer
Uriel Pharmacy, Inc.
Effective date
2022-10-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:18:17

Label at a glance#

ProductRobinia Nicotiana
Active ingredientSTRYCHNOS NUX-VOMICA SEED, COPPER, SILVER, SODIUM PHOSPHATE, TOBACCO LEAF, ROBINIA PSEUDOACACIA BARK, BOS TAURUS ADRENAL GLAND
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: Robinia 4X, Argentum nitricum (Silver nitrate) 6X, Nicotiana (Tobacco) 6X, Nux vomica (Poison nut) 6X,
Gl. suprarenales (Bovine adrenal gland) 8X, Cuprum met. (Copper) 8X, Natrium phos. (Sodium monohydrogenphosphate) 10X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Salt

OTC - PURPOSE SECTION

Use: Temporary relief of upset stomach.

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. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Robinia Nicotiana AmpulesRobinia Nicotiana Ampules

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c599c4a0-705d-4ebb-ab1f-977af038f96aProduct name120251124
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8395-1Robinia Nicotiana1 mL in 1 AMPULELIQUID11
48951-8395-1Robinia Nicotiana10 in 1 BOXLIQUID101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8395ROBINIA NICOTIANA LIQUID [URIEL PHARMACY, INC.]1Legacy NDC, 2 package rows20221014_eadc50f4-5721-2a2a-e053-2995a90a8559.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-839548951-8395-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

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
eadc50f4-5722-2a2a-e053-2995a90a8559eadc50f4-5721-2a2a-e053-2995a90a85592022-10-12WarningsExact identifier
spl id: eadc50f4-5722-2a2a-e053-2995a90a8559
spl set id: eadc50f4-5721-2a2a-e053-2995a90a8559

Reported adverse events (FAERS/openFDA)#

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