Purpose
Uses: For healthy teeth and bone development.
Osteodoron Pm Bone Support
FDA Label NDC 48951-7097
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Uriel Pharmacy Inc for the product Osteodoron Pm Bone Support (NDC 48951-7097). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding purpose, dosage & administration, otc-active ingredient, inactive ingredient, keep out of reach of children, do not use section, ask doctor section, pregnancy or breast feeding section, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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 53120www.urielpharmacy.com
Principal Display Panel
Osteodoron PM
Bone Support Powder
Homeopathic
net vol. 60 ml (2 fl. oz.)
Osteodoron Pm Powder Bottle Label (Ostpmp01)
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