FDA.reportPublic FDA data

Periodontium Quartz

Manufacturer
Uriel Pharmacy, Inc.
Effective date
2024-10-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:28:23

Label at a glance#

ProductPeriodontium Quartz
Active ingredientSUS SCROFA TOOTH, SILICA, ATROPA BELLADONNA, BEEF TONGUE, CALENDULA OFFICINALIS FLOWERING TOP, BOS TAURUS BONE, SILVER NITRATE
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: Calendula 3X, Atropa belladonna (Nightshade) 17X, Gingiva (Bovine gums) 17X, Mandibula -feti (Bovine fetal lower jaw) 17X, Maxilla - feti (Bovine fetal upper jaw) 17X, Periodontium (Bovine connective tissue, socket and gums of teeth) 17X, Argentum nitricum (Silver nitrate) 20X, Quartz (Rock crystal) 30X,

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled water, 20% Organic cane alcohol

Prepared using rhythmical processes

OTC - PURPOSE SECTION

Use: Temporary relief of headache.

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. 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

Periodontium Quartz LiquidPeriodontium Quartz Liquid

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8415-3Periodontium Quartz60 mL in 1 BOTTLE, DROPPERLIQUID601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8415PERIODONTIUM QUARTZ LIQUID [URIEL PHARMACY, INC.]11 package rows20241027_253b9c91-df3e-b0b3-e063-6294a90a669a.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-841548951-8415-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SUS SCROFA TOOTHV69U5FL51FACTIB
SILICAETJ7Z6XBU4ACTIB
ATROPA BELLADONNAWQZ3G9PF0HACTIB
BEEF TONGUE4LKR3JG619ACTIB
CALENDULA OFFICINALIS FLOWERING TOP18E7415PXQACTIB
BOS TAURUS BONETRS31EO6ZNACTIB
SILVER NITRATE95IT3W8JZEACTIB
ALCOHOL3K9958V90MIACT

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
253b9c91-df3f-b0b3-e063-6294a90a669a253b9c91-df3e-b0b3-e063-6294a90a669a2024-10-24WarningsExact identifier
spl id: 253b9c91-df3f-b0b3-e063-6294a90a669a
spl set id: 253b9c91-df3e-b0b3-e063-6294a90a669a

Reported adverse events (FAERS/openFDA)#

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