Magnesia Muriatica
FDA Label NDC 10191-1973
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Remedy Makers for the product Magnesia Muriatica (NDC 10191-1973). 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 otc - purpose, otc - active ingredient, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
Otc - Keep Out Of Reach Of Children
Indications & Usage
Warnings
WARNING: Use only if cap and seal are unbroken. If symptoms persist for more than 3 days or worsen, discontinue (STOP) use and consult your physician. As with any drug. If you are pregnant or nursing (breast-feeding) a baby, seek the advise of a health professional before using this product. Store tightly closed in a cool area.
Dosage & Administration
Inactive Ingredient
Inactive Ingredient: Lactose and Sucrose. Free from yeast, wheat, corn and soy.
Otc - Questions
Questions or comments.(877)REM4YOU. Fax (909)594-4205 Pomona, CA. 91768. USA www.remedymakers.com
Other information: Contain approx.139 - 148 pellets.
Package Label.Principal Display Panel
* Please review the disclaimer below.