FDA.reportPublic FDA data

Robinia Nicotianna

Manufacturer
Uriel Pharmacy, Inc.
Effective date
2022-10-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:52:32

Label at a glance#

ProductRobinia Nicotianna
Active ingredientCOPPER, SODIUM PHOSPHATE, SILVER, ROBINIA PSEUDOACACIA BARK, STRYCHNOS NUX-VOMICA SEED, SUS SCROFA ADRENAL GLAND, TOBACCO LEAF
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.

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: Distilled water, 20% Organic cane alcohol, Lactose

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. Contains traces of lactose. 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.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
shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Robinia Nicotiana LiquidRobinia Nicotiana Liquid

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
48951-839448951-8394-3

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
COPPER789U1901C5ACTIB
SODIUM PHOSPHATESE337SVY37ACTIB
WATER059QF0KO0RIACT
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT
ALCOHOL3K9958V90MIACT
SILVER3M4G523W1GACTIB
ROBINIA PSEUDOACACIA BARK7TPC058OWYACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
SUS SCROFA ADRENAL GLAND398IYQ16YVACTIB
TOBACCO LEAF6YR2608RSUACTIB

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
eaed01cf-b62d-8627-e053-2a95a90aa2e1ea274431-c12d-e79c-e053-2995a90adbec2022-10-13WarningsExact identifier
spl set id: ea274431-c12d-e79c-e053-2995a90adbec