OSTEODORON PM BONE SUPPORT- oyster shell calcium carbonate, crude white oak bark calcium fluoride silicon dioxide powder

Osteodoron PM Bone Support by

Drug Labeling and Warnings

Osteodoron PM Bone Support by is a Homeopathic medication manufactured, distributed, or labeled by Uriel Pharmacy Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Purpose

Uses: For healthy teeth and bone development.

Dosage & Administration

Directions: Take in the evening. Use with Osteodoron AM Bone Support Powder. Ages 12 and older:  1/8 tsp. Ages 2-11:  1/16 tsp. Under age 2: Ask a doctor.

OTC-Active Ingredient

Active Ingredients:  Conchae 1X HPUS, Quercus e cort. 4X HPUS, Fluorite 6X HPUS, Quartz 6X HPUS.

Inactive Ingredient

Inactive Ingredient: Lactose

Keep out of reach of children

KEEP OUT OF REACH OF CHILDREN.

Do not use section

Warnings:  Do not use if allergic to any ingredient. Do not use if safety seal is broken or missing.

Ask doctor section

Consult your doctor if you are lactose intolerant, or if inadequate dietary calcium is a concern. When using this product, consult your doctor regularly to ensure that improvement is proceeding normally.

Pregnancy or breast feeding section

If you are pregnant or nursing, consult a doctor before use.

Questions section

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

Principal Display Panel

Osteodoron PM

Bone Support Powder

Homeopathic

net vol. 60 ml (2 fl. oz.)

INGREDIENTS AND APPEARANCE

OSTEODORON PM BONE SUPPORT 
oyster shell calcium carbonate, crude white oak bark calcium fluoride silicon dioxide powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 48951-7097
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I)	OYSTER SHELL CALCIUM CARBONATE, CRUDE	1 [hp_X]
WHITE OAK BARK (UNII: 93LP7Y8EGT) (WHITE OAK BARK - UNII:93LP7Y8EGT)	WHITE OAK BARK	4 [hp_X]
CALCIUM FLUORIDE (UNII: O3B55K4YKI) (CALCIUM FLUORIDE - UNII:O3B55K4YKI)	CALCIUM FLUORIDE	6 [hp_X]
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	6 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
LACTOSE (UNII: J2B2A4N98G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48951-7097-4	1 in 1 BOTTLE, GLASS

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		09/01/2009

Labeler - Uriel Pharmacy Inc (043471163)

Establishment
Name	Address	ID/FEI	Business Operations
Uriel Pharmacy Inc		043471163	manufacture