Indications & Usage
Directions: FOR ORAL USE ONLY.
Periodontium Hypophysis
FDA Label NDC 48951-8016
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 Periodontium Hypophysis (NDC 48951-8016). 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 indications & usage, dosage & administration, otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, warnings, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Dosage & Administration
Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.
Otc - Active Ingredient
Active Ingredients: Gingiva (Bovine gums) 8X, Hypophysis (Bovine pituitary gland) 8X, Mandibula - feti (Bovine fetal lower jaw) 8X, Maxilla - feti (Bovine fetal upper jaw) 8X, Periodontium (Bovine connective tissue, socket and gums of teeth) 8X, Stannum met. (Metallic tin) 17X
Inactive Ingredient
Inactive Ingredients: Water, Salt
Otc - Purpose
Use: Temporary relief of headache.
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
Warnings
Warnings: Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Natural ingredients may cause color, scent and/or taste variation.
Otc - Questions
Questions? Call 866.642.2858 Uriel, East Troy, WI 53120 www.urielpharmacy.com
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