Pulpa Dentis 30 Special Order
- Manufacturer
- Uriel Pharmacy Inc.
- Effective date
- 2018-05-08
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 00:58:51
Label at a glance#
ProductPulpa Dentis 30 Special Order
Active ingredientSUS SCROFA TOOTH
Label structure9 sections
Contacts and useful links#
Websitewww.urielpharmacy.com
www.urielpharmacy.com
www.urielpharmacy.comLabel 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 Ingredient: Pulpa dentis (Bovine dental pulp) 30X
INACTIVE INGREDIENT SECTION
Inactive Ingredient: Distilled water
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.
REFRIGERATE AFTER OPENING.
BEST WHEN USED WITHIN 90 DAYS OF OPENING.
OTC - QUESTIONS SECTION
Questions? Call 866.642.2858
Made with care by Uriel, East Troy, WI 53120
www.urielpharmacy.com
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Products#
Every source-derived product name is available through these pages.
- Pulpa Dentis 30 Special Order
- SUS SCROFA TOOTH
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-8324 | 48951-8324-3 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SUS SCROFA TOOTH | V69U5FL51F | ACTIB |
| WATER | 059QF0KO0R | 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 |
|---|---|---|---|---|---|---|
| b5e4a905-64b7-48eb-e053-2a95a90afc52 | 6bb49103-4a83-4cfc-e053-2991aa0a51ae | 2020-12-07 | Warnings | 6bb49103-4a83-4cfc-e053-2991aa0a51ae |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.