OSTEODORON PM powder

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4), OSTREA EDULIS SHELL (UNII: 49OY13BE7Z) (OSTREA EDULIS SHELL - UNII:49OY13BE7Z), QUERCUS ROBUR WHOLE (UNII: R7QMG0BT2W) (QUERCUS ROBUR WHOLE - UNII:R7QMG0BT2W), CALCIUM FLUORIDE (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O)

Available from:

Uriel Pharmacy Inc.

Administration route:

ORAL

Prescription type:

OTC DRUG

Therapeutic indications:

Directions: FOR ORAL USE ONLY. Use: For healthy bone and teeth development.

Authorization status:

unapproved homeopathic

Summary of Product characteristics

OSTEODORON PM- OSTEODORON PM 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._
----------
OSTEODORON PM
Directions: FOR ORAL USE ONLY.
Take in the evening. Use in combination with Osteodoron AM Bone
Support Powder.
Ages 12 and older: 1/8 teaspoon. Ages 2-11: 1/16 teaspoon. Under age
2: Consult a
doctor.
Active Ingredients: 100 gm contains: 5gm Conchae (Oyster shells) 1X;
Quercus (Oak)
4X, Fluorite (Calcium fluoride) 6X, Quartz (Rock crystal) 6X
Inactive Ingredient: Lactose
"prepared using rhythmical processes"
Use: 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 PM
osteodoron pm powder
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:48951-7191
ROUTE OF ADMINISTRATION
ORAL
Uriel Pharmacy Inc.
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF
STRENGTH
STRENGTH
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)
SILICON DIOXIDE
6 [hp_X]
in 1 g
OSTREA EDULIS SHELL (UNII: 49OY13BE7Z) (OSTREA EDULIS SHELL -
UNII:49OY13BE7Z )
OSTREA EDULIS
SHELL
1 [hp_X]
in 1 g
QUERCUS ROBUR WHOLE (UNII: R7QMG0BT2W) (QUERCUS ROBUR WHOLE -
UNII:R7QMG0BT2W)
QUERCUS ROBUR
WHOLE
4 [hp_X]
in 1 g
CALCIUM FLUORIDE (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O)
CALCIUM FLUORIDE
6 [hp_X]
in 1 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)
PACKAGING
# ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END