OSTEODORON AM powder

Pajjiż: Stati Uniti

Lingwa: Ingliż

Sors: NLM (National Library of Medicine)

Ixtrih issa

Ingredjent attiv:

CUCURBITA PEPO FLOWER (UNII: 413MGP37HQ) (CUCURBITA PEPO FLOWER - UNII:413MGP37HQ), CALCIUM FLUORIDE (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O), SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4), FLUORAPATITE (UNII: M4CM1H238J) (FLUORAPATITE - UNII:M4CM1H238J)

Disponibbli minn:

Uriel Pharmacy Inc.

Rotta amministrattiva:

ORAL

Tip ta 'preskrizzjoni:

OTC DRUG

Indikazzjonijiet terapewtiċi:

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

L-istatus ta 'awtorizzazzjoni:

unapproved homeopathic

Karatteristiċi tal-prodott

                                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._
----------
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
osteodoron am powder
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:48951-7190
ROUTE OF ADMINISTRATION
ORAL
Uriel Pharmacy Inc.
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF
STRENGTH
STRENGTH
CUCURBITA PEPO FLOWER (UNII: 413MGP37HQ) (CUCURBITA PEPO FLOWER -
UNII:413MGP37HQ)
CUCURBITA PEPO
FLOWER
3 [hp_X]
in 1 g
CALCIUM FLUORIDE (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O)
CALCIUM FLUORIDE
6 [hp_X]
in 1 g
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)
SILICON DIOXIDE
6 [hp_X]
in 1 g
FLUORAPATITE (UNII: M4CM1H238J) (FLUORAPATITE - UNII:M4CM1H238J)
FLUORAPATITE
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
DATE
1
NDC:48951-
7190-4
50 g 
                                
                                Aqra d-dokument sħiħ
                                
                            

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