FDA.reportPublic FDA data

Osteodoron AM Special Formula

Manufacturer
Uriel Pharmacy Inc.
Effective date
2024-01-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:25:42

Label at a glance#

ProductOsteodoron AM Special Formula
Active ingredientCUCURBITA PEPO FLOWER, FLUORAPATITE, CALCIUM FLUORIDE, SILICON DIOXIDE, LEAD CARBONATE
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Take in the morning. Use in combination with Osteodoron PM Special Formula Powder. Ages 12 and older: 1/8 teaspoon. Ages 2-11: 1/16 teaspoon. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Cucurbita (Squash) 3X, Apatite (Nat. calcium fluorophosphate) 6X, Fluorite (Calcium fluoride) 6X, Quartz (Rock crystal) 6X, Cerussite (White lead ore) 8X

INACTIVE INGREDIENT SECTION

Inactive Ingredient: Lactose

OTC - PURPOSE SECTION

Use: For healthy teeth and bone development.

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 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 Uriel, East Troy, WI 53120 shopuriel.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Osteodoron AM Special Formula PowderOsteodoron AM Special Formula Powder

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-7202-4Osteodoron AM Special Formula50 g in 1 BOTTLE, GLASSPOWDER501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-7202OSTEODORON AM SPECIAL FORMULA POWDER [URIEL PHARMACY INC.]11 package rows20240118_0f2963d0-5392-cfd7-e063-6394a90ab7ee.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-720248951-7202-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
CUCURBITA PEPO FLOWER413MGP37HQACTIB
FLUORAPATITEM4CM1H238JACTIB
CALCIUM FLUORIDEO3B55K4YKIACTIB
LACTOSEJ2B2A4N98GIACT
SILICON DIOXIDEETJ7Z6XBU4ACTIB
LEAD CARBONATE43M0P24L2BACTIB

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
0f2961b0-3cba-d136-e063-6394a90aa1420f2963d0-5392-cfd7-e063-6394a90ab7ee2024-01-17WarningsExact identifier
spl id: 0f2961b0-3cba-d136-e063-6394a90aa142
spl set id: 0f2963d0-5392-cfd7-e063-6394a90ab7ee

Reported adverse events (FAERS/openFDA)#

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