Otc - Active Ingredient
SILICON DIOXIDE
Silicea Pellet
FDA Label NDC 71919-827
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Washington Homeopathic Products for the product Silicea (NDC 71919-827). 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 - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, 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
Otc - Purpose
Indicated for Formation of pus
Otc - Keep Out Of Reach Of Children
As with all medicines, keep out of reach of children.
Indications & Usage
SILICEA Formation of pus
Warnings
If symptoms worsen or persist for more than 7 days, or if pregnant or nursing, consult a licensed practitioner.
Dosage & Administration
Directions: Adults & children: Dissolve 4 pellets under the tongue 3 times a day or as directed by a licensed practitioner. Other information: Do not use if seal is broken.
Inactive Ingredient
SUCROSE/LACTOSE
Package Label.Principal Display Panel
The OTC potency range of Silicea is 30c - 200c.
Availability is subject to change.
Silicea-4dram (Silicea)
* Please review the disclaimer below.
