OSTEODORON AM- osteodoron am 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

Directions: FOR ORAL USE ONLY.

Take in the morning. Use in combination with Osteodoron PM 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

Inactive Ingredient: Lactose

prepared using rhythmical processes

Uses: For healthy bone and teeth 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
shopuriel.com Lot:

Osteodoron AM Powder

OSTEODORON AM 
osteodoron am powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-7190
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
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
FLUORAPATITE (UNII: M4CM1H238J) (FLUORAPATITE - UNII:M4CM1H238J) FLUORAPATITE6 [hp_X]  in 1 g
Inactive Ingredients
Ingredient NameStrength
LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48951-7190-450 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(48951-7190)

Revised: 4/2024
Document Id: 15ae0c22-7989-149f-e063-6294a90a7551
Set id: 97e1871e-7f89-4dbd-e053-2a95a90a1153
Version: 3
Effective Time: 20240409
 
Uriel Pharmacy Inc.