Indications & Usage
Directions: FOR ORAL USE.
Secale Argentum Special Order
FDA Label NDC 48951-8172
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 Secale Argentum Special Order (NDC 48951-8172). 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, package label.principal display panel, 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: Aristolochia ex herba 3X, Pulsatilla e flor. 6X, Secale corn. e grano 6X, Argentum metallicum 8X
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 of if conditions worsen or persist. If pregnant or nursing, consult a doctor before use.
* Please review the disclaimer below.
