Stibium 6 Liquid
FDA Label NDC 48951-8213

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 Stibium 6 (NDC 48951-8213). 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

Indications & Usage

Directions: FOR ORAL USE.

Dosage & Administration

Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.

Otc - Active Ingredient

Active Ingredient: Stibium met. (Antimony) 6X

Inactive Ingredient

Inactive Ingredients: Water, Salt, Lactose

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. Contains traces of lactose. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use.

Otc - Questions

Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
www.urielpharmacy.com

* Please review the disclaimer below.