OSTEODORON AM SPECIAL FORMULA- osteodoron am special formula 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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Osteodoron AM Special Formula

Directions: FOR ORAL USE ONLY.

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.

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: 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

OsteodoronAMSpecialFormulaPowder

OSTEODORON AM SPECIAL FORMULA 
osteodoron am special formula powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-7115
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CUCURBITA PEPO FLOWER (UNII: 413MGP37HQ) (CUCURBITA PEPO FLOWER - UNII:413MGP37HQ) CUCURBITA PEPO FLOWER3 [hp_X]  in 1 g
FLUORAPATITE (UNII: M4CM1H238J) (FLUORAPATITE - UNII:M4CM1H238J) FLUORAPATITE6 [hp_X]  in 1 g
CALCIUM FLUORIDE (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O) CALCIUM FLUORIDE6 [hp_X]  in 1 g
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE6 [hp_X]  in 1 g
LEAD CARBONATE (UNII: 43M0P24L2B) (LEAD - UNII:2P299V784P) LEAD CARBONATE8 [hp_X]  in 1 g
Inactive Ingredients
Ingredient NameStrength
LACTOSE (UNII: J2B2A4N98G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48951-7115-460 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(48951-7115)

Revised: 4/2018
Document Id: 6ad9967f-be68-1066-e053-2a91aa0abd95
Set id: 8c69d605-cdcf-4560-9f2a-446cf334b81c
Version: 3
Effective Time: 20180427
 
Uriel Pharmacy Inc.