Osteodoron PM
- Manufacturer
- Uriel Pharmacy Inc.
- Effective date
- 2024-12-16
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- full-release
- Hydrated at
- 2026-06-01 02:29:39
Label at a glance#
ProductOsteodoron PM
Active ingredientOSTREA EDULIS SHELL, SILICON DIOXIDE, QUERCUS ROBUR WHOLE, CALCIUM FLUORIDE
Label structure9 sections
Contacts and useful links#
Label contents#
Full prescribing information#
INDICATIONS & USAGE SECTION
Directions: FOR ORAL USE ONLY.
DOSAGE & ADMINISTRATION SECTION
Take in the evening. Use in combination with Osteodoron AM Bone Support 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: 100 gm contains: 5gm Conchae (Oyster shells) 1X; Quercus (Oak) 4X, Fluorite (Calcium fluoride) 6X, Quartz (Rock crystal) 6X
INACTIVE INGREDIENT SECTION
Inactive Ingredient: Lactose
Prepared using rhythmical processes.
OTC - PURPOSE SECTION
Use: For healthy bone and teeth 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 Lot:
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-7191-4 | Osteodoron PM | 50 g in 1 BOTTLE, GLASS | POWDER | 50 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-7191 | OSTEODORON PM POWDER [URIEL PHARMACY INC.] | 4 | Legacy NDC, 1 package rows | 20241218_97dec905-12d6-4b5d-e053-2a95a90a6bac.zip |
Products#
Every source-derived product name is available through these pages.
- Osteodoron PM
- OSTREA EDULIS SHELL
- SILICON DIOXIDE
- QUERCUS ROBUR WHOLE
- LACTOSE, UNSPECIFIED FORM
- ANHYDROUS LACTOSE
- CALCIUM FLUORIDE
- FLUORIDE ION
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-7191 | 48951-7191-4 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| OSTREA EDULIS SHELL | 49OY13BE7Z | ACTIB |
| SILICON DIOXIDE | ETJ7Z6XBU4 | ACTIB |
| QUERCUS ROBUR WHOLE | R7QMG0BT2W | ACTIB |
| LACTOSE, UNSPECIFIED FORM | J2B2A4N98G | IACT |
| CALCIUM FLUORIDE | O3B55K4YKI | 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 |
|---|---|---|---|---|---|---|
| 2967954a-840f-65c7-e063-6394a90ac1a0 | 97dec905-12d6-4b5d-e053-2a95a90a6bac | 2024-12-16 | Warnings | 2967954a-840f-65c7-e063-6394a90ac1a0 97dec905-12d6-4b5d-e053-2a95a90a6bac |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.