Robinia Nicotiana
- Manufacturer
- Uriel Pharmacy, Inc.
- Effective date
- 2023-11-03
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 02:23:03
Label at a glance#
Contacts and useful links#
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
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| c599c4a0-705d-4ebb-ab1f-977af038f96a | Product name | 1 | 20251124 |
| efd58dcf-540a-4531-8766-e713129ca6f2 | Product name | 1 | 20250307 |
| 4b7700e3-6e0e-45e5-9d22-6f754d61386e | Product name | 2 | 20250304 |
| 726062af-1135-4707-a1d7-57256991bbf9 | Product name | 2 | 20250226 |
| 7cda52fc-125f-421c-8fea-bc1974370c49 | Product name | 2 | 20180703 |
| 0ca1d589-929b-4b33-bc5b-1d84abdafa6a | Product name | 1 | 20150324 |
| fc363c46-397b-4476-ac0f-70e43e8e4592 | Product name | 1 | 20150324 |
| 19c71a3d-ed9c-166b-a7e5-38c250c35631 | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-8397-3 | Robinia Nicotiana | 60 mL in 1 BOTTLE, GLASS | LIQUID | 60 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-8397 | ROBINIA NICOTIANA LIQUID [URIEL PHARMACY, INC.] | 2 | Legacy NDC, 1 package rows | 20231104_eaed2e4b-d6bf-2e8d-e053-2995a90a1985.zip |
Products#
Every source-derived product name is available through these pages.
- Robinia Nicotiana
- TOBACCO LEAF
- STRYCHNOS NUX-VOMICA SEED
- LACTOSE, UNSPECIFIED FORM
- WATER
- BOS TAURUS ADRENAL GLAND
- ALCOHOL
- COPPER
- SODIUM PHOSPHATE
- PHOSPHATE ION
- ROBINIA PSEUDOACACIA BARK
- SILVER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-8397 | 48951-8397-3 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| TOBACCO LEAF | 6YR2608RSU | ACTIB |
| STRYCHNOS NUX-VOMICA SEED | 269XH13919 | ACTIB |
| LACTOSE, UNSPECIFIED FORM | J2B2A4N98G | IACT |
| WATER | 059QF0KO0R | IACT |
| BOS TAURUS ADRENAL GLAND | M2776SWB29 | ACTIB |
| ALCOHOL | 3K9958V90M | IACT |
| COPPER | 789U1901C5 | ACTIB |
| SODIUM PHOSPHATE | SE337SVY37 | ACTIB |
| ROBINIA PSEUDOACACIA BARK | 7TPC058OWY | ACTIB |
| SILVER | 3M4G523W1G | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 0945d7ce-ca9f-b45a-e063-6294a90a6a54 | eaed2e4b-d6bf-2e8d-e053-2995a90a1985 | 2023-11-03 | Warnings | 0945d7ce-ca9f-b45a-e063-6294a90a6a54 eaed2e4b-d6bf-2e8d-e053-2995a90a1985 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
