Indications & Usage
Directions: FOR RECTAL USE.
Argentum 0.4% Adult
FDA Label NDC 48951-1371
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 Argentum 0.4% Adult (NDC 48951-1371). 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
Insert 1 suppository as needed.
Otc - Active Ingredient
Active Ingredient: 100 gm contains:
4 gm Argentum met. (Silver) 1X
Inactive Ingredient
Inactive Ingredients: Cocoa butter, Micronized silica gel
"prepared using rhythmical processes"
Otc - Purpose
Use: Temporary relief of headache.
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
Warnings
Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. 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. Do not use if safety seals on box are broken or missing.
KEEP REFRIGERATED OR STORE IN COOL, DRY PLACE.
REFRIGERATE TO RESOLIDIFY.
Otc - Questions
Questions? Call 866.642.2858 Uriel, East Troy, WI 53120 shopuriel.com Lot:
* Please review the disclaimer below.
