Echinacea Quartz
- Manufacturer
- Uriel Pharmacy, Inc.
- Effective date
- 2024-11-22
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-06-01 02:29:03
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
INDICATIONS & USAGE SECTION
Directions: FOR TOPICAL USE ONLY.
DOSAGE & ADMINISTRATION SECTION
Apply to gums and inside of mouth as needed. Under age 2: Consult a doctor.
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients: 100 gm contains: 89 gm Althaea (Marsh mallow root) 2X; Echinacea (Purple coneflower) 2X, Antimonite (Nat. antimony trisulfide) 5X, Argentum nitricum (Silver nitrate) 20X, Atropa belladonna (Nightshade) 20X, Quartz (Rock crystal) 20X
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Spring water, Distilled water, Boric acid, Glycerin, Sodium alginate, Sodium hydroxide, Sorbic acid, Tea tree oil, Chlorophyll, Stevioside, Grapefruit seed extract, Rose oil
Prepared using rhythmical processes.
OTC - PURPOSE SECTION
Uses: Temporarily relieves symptoms of hypersensitive teeth, gum inflammation, soreness or dryness in the mouth and may be used before and after dental work.
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. Avoid contact with eyes. 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 Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-4172-5 | Echinacea Quartz | 60 g in 1 TUBE | GEL | 60 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-4172 | ECHINACEA QUARTZ GEL [URIEL PHARMACY, INC.] | 3 | Legacy NDC, 1 package rows | 20241123_e2972b6d-7246-712f-e053-2995a90a09b9.zip |
Products#
Every source-derived product name is available through these pages.
- Echinacea Quartz
- SILVER
- GLYCERIN
- SODIUM ALGINATE
- TEA TREE OIL
- SORBIC ACID
- CITRUS PARADISI SEED
- STEVIOSIDE
- ECHINACEA, UNSPECIFIED
- ANTIMONY TRISULFIDE
- ATROPA BELLADONNA
- SILICON DIOXIDE
- WATER
- BORIC ACID
- SODIUM HYDROXIDE
- ROSE OIL
- ALTHAEA OFFICINALIS ROOT
- CHLOROPHYLL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-4172 | 48951-4172-5 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SILVER | 3M4G523W1G | ACTIB |
| GLYCERIN | PDC6A3C0OX | IACT |
| SODIUM ALGINATE | C269C4G2ZQ | IACT |
| TEA TREE OIL | VIF565UC2G | IACT |
| SORBIC ACID | X045WJ989B | IACT |
| CITRUS PARADISI SEED | 12F08874Y7 | IACT |
| STEVIOSIDE | 0YON5MXJ9P | IACT |
| ECHINACEA, UNSPECIFIED | 4N9P6CC1DX | ACTIB |
| ANTIMONY TRISULFIDE | F79059A38U | ACTIB |
| ATROPA BELLADONNA | WQZ3G9PF0H | ACTIB |
| SILICON DIOXIDE | ETJ7Z6XBU4 | ACTIB |
| WATER | 059QF0KO0R | IACT |
| BORIC ACID | R57ZHV85D4 | IACT |
| SODIUM HYDROXIDE | 55X04QC32I | IACT |
| ROSE OIL | WUB68Y35M7 | IACT |
| ALTHAEA OFFICINALIS ROOT | TRW2FUF47H | ACTIB |
| CHLOROPHYLL | 00WNZ48OR9 | IACT |
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 |
|---|---|---|---|---|---|---|
| 27847d56-f1e5-53e7-e063-6394a90a82c2 | e2972b6d-7246-712f-e053-2995a90a09b9 | 2024-11-22 | Warnings | 27847d56-f1e5-53e7-e063-6394a90a82c2 e2972b6d-7246-712f-e053-2995a90a09b9 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
