FDA.reportPublic FDA data

Robinia Nicotiana

Manufacturer
Uriel Pharmacy Inc.
Effective date
2021-05-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:14:34

Label at a glance#

ProductRobinia Nicotiana
Active ingredientROBINIA PSEUDOACACIA BARK, SILVER, SUS SCROFA ADRENAL GLAND, TOBACCO LEAF, STRYCHNOS NUX-VOMICA SEED, COPPER, SODIUM PHOSPHATE
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Dissolve pellets under the tongue 3-4 times daily. Ages 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Robinia 4X, Argentum nitricum (Silver nitrate) 6X, Gl. suprarenales sinistra (Bovine left adrenal gland) 8X, Nicotiana (Tobacco) 6X, Nux vomica (Poison nut) 6X, Cuprum met. (Copper) 8X, Natrium phosphoricum (Sodium monohydrogenphosphate) 10X

INACTIVE INGREDIENT SECTION

Inactive Ingredient: Sucrose

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. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. 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. Do not use if safety seal is broken or missing.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Robinia Nicotiana PelletsRobinia Nicotiana Pellets

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
48951-8374-22026-01-29C16284748780-149896155-a5cf-586f-e063-e6dba90add90Robinia Nicotiana

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8374-2Robinia Nicotiana1350 in 1 BOTTLE, GLASSPELLET13501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8374ROBINIA NICOTIANA PELLET [URIEL PHARMACY INC.]1Legacy NDC, 1 package rows20210529_c364df2d-8973-3872-e053-2995a90aa3de.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-837448951-8374-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUCROSEC151H8M554IACT
ROBINIA PSEUDOACACIA BARK7TPC058OWYACTIB
SILVER3M4G523W1GACTIB
SUS SCROFA ADRENAL GLAND398IYQ16YVACTIB
TOBACCO LEAF6YR2608RSUACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
COPPER789U1901C5ACTIB
SODIUM PHOSPHATESE337SVY37ACTIB

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
c364e01a-5e57-509e-e053-2a95a90a3c89c364df2d-8973-3872-e053-2995a90aa3de2021-05-27WarningsExact identifier
spl id: c364e01a-5e57-509e-e053-2a95a90a3c89
spl set id: c364df2d-8973-3872-e053-2995a90aa3de

Reported adverse events (FAERS/openFDA)#

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