APATITE CUCURBITA- apatite cucurbita powder 
Uriel Pharmacy Inc.

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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Apatite Cucurbita

Directions: FOR ORAL USE ONLY.

Take 3-4 times daily. Ages 12 and older: 1/8 teaspoon. Ages 2-11: 1/16 teaspoon. Under age 2: Consult a doctor.

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

Inactive Ingredient: Lactose

Use: For healthy teeth and bone development.

KEEP OUT OF REACH OF CHILDREN.

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.

Questions? Call 866.642.2858 Uriel, East Troy, WI 53120 www.urielpharmacy.com

ApatiteCucurbitaPowder

APATITE CUCURBITA 
apatite cucurbita powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-1041
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CUCURBITA PEPO FLOWER (UNII: 413MGP37HQ) (CUCURBITA PEPO FLOWER - UNII:413MGP37HQ) CUCURBITA PEPO FLOWER3 g  in 1 g
FLUORAPATITE (UNII: M4CM1H238J) (FLUORAPATITE - UNII:M4CM1H238J) FLUORAPATITE6 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
LACTOSE (UNII: J2B2A4N98G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48951-1041-450 g in 1 BOTTLE, GLASS; Type 0: Not a Combination Product09/01/2009
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic09/01/2009
Labeler - Uriel Pharmacy Inc. (043471163)
Establishment
NameAddressID/FEIBusiness Operations
Uriel Pharmacy Inc.043471163manufacture(48951-1041)

Revised: 4/2018
Document Id: 698408a5-520d-2854-e053-2991aa0a53f8
Set id: 518a0ee9-00a7-4aaf-b811-11ef6c182d7c
Version: 4
Effective Time: 20180410
 
Uriel Pharmacy Inc.