Phosphorus Tartarus
- Manufacturer
- Uriel Pharmacy Inc.
- Effective date
- 2024-01-18
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:25:45
Label at a glance#
ProductPhosphorus Tartarus
Active ingredientANTIMONY POTASSIUM TARTRATE, PHOSPHORUS
Label structure9 sections
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: Tartarus stibiatus (Potassium antimonotartrate) 3X, Phosphorus (Yellow phosphorus) 6X
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Distilled water, Organic cane alcohol, Lactose
"prepared using rhythmical processes"
OTC - PURPOSE SECTION
Use: Temporary relief of cough.
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. 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
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 7792dadb-52b6-46b6-8fdf-80b1171065b5 | Product name | 1 | 20180810 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-8406-3 | Phosphorus Tartarus | 60 mL in 1 BOTTLE, DROPPER | LIQUID | 60 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-8406 | PHOSPHORUS TARTARUS LIQUID [URIEL PHARMACY INC.] | 1 | 1 package rows | 20240120_0f4e49fa-6bb4-c9de-e063-6294a90a5f64.zip |
Products#
Every source-derived product name is available through these pages.
- Phosphorus Tartarus
- WATER
- ALCOHOL
- LACTOSE
- ANTIMONY POTASSIUM TARTRATE
- ANTIMONY CATION (3+)
- PHOSPHORUS
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-8406 | 48951-8406-3 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| LACTOSE | J2B2A4N98G | IACT |
| ANTIMONY POTASSIUM TARTRATE | DL6OZ476V3 | ACTIB |
| PHOSPHORUS | 27YLU75U4W | 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 |
|---|---|---|---|---|---|---|
| 0f4e4a0d-ed4e-5216-e063-6394a90a8634 | 0f4e49fa-6bb4-c9de-e063-6294a90a5f64 | 2024-01-18 | Warnings | 0f4e4a0d-ed4e-5216-e063-6394a90a8634 0f4e49fa-6bb4-c9de-e063-6294a90a5f64 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.