Apatite Cucurbita

Manufacturer: Uriel Pharmacy Inc.
Effective date: 2024-12-17
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:29:43

Label at a glance#

ProductApatite Cucurbita

Active ingredientCUCURBITA PEPO FLOWER, FLUORAPATITE

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

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: 1/8 teaspoon. Ages 2-11: 1/16 teaspoon. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Cucurbita (Pumpkin) 3X, Apatite (Nat. calcium fluorophosphate) 6X

INACTIVE INGREDIENT SECTION

Inactive Ingredient: Lactose

Prepared using rhythmical processes.

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 Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Apatite Cucurbita Powder

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-1386-4	Apatite Cucurbita	50 g in 1 BOTTLE, GLASS	POWDER	50		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-1386	APATITE CUCURBITA POWDER [URIEL PHARMACY INC.]	1	1 package rows	20241220_298df27b-d5e5-a559-e063-6394a90a6e34.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Apatite Cucurbita
LACTOSE
CUCURBITA PEPO FLOWER
FLUORAPATITE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-1386	48951-1386-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
LACTOSE	J2B2A4N98G	IACT
CUCURBITA PEPO FLOWER	413MGP37HQ	ACTIB
FLUORAPATITE	M4CM1H238J	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
298df551-3385-a7c1-e063-6394a90ac1c6			298df27b-d5e5-a559-e063-6394a90a6e34	2024-12-17	Warnings	Exact identifier spl id: 298df551-3385-a7c1-e063-6394a90ac1c6 spl set id: 298df27b-d5e5-a559-e063-6394a90a6e34

Reported adverse events (FAERS/openFDA)#

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