Silica
FDA Label NDC 48951-8317

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 Silica (NDC 48951-8317). 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 purpose, dosage & administration, otc-active ingredient, inactive ingredient, keep out of reach of children, do not use if allergic to any ingredient. do not use if safety seal is broken or missing., ask doctor section, pregnancy or breast feeding section, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Purpose

Uses: To promote skin elasticity and strengthen hair and nails.

Dosage & Administration

Directions: Take regularly before meals with a small amount of water. Ages 12 and older: 1 tsp. Ages 2-11: 1/2 tsp.   Under age 2: Ask a doctor.

Inactive Ingredient

Inactive Ingredients: Lactose, Bee pollen, Diatomaceous earth, Anise oil, Mesenchyme, Pancreas, Pulmo, Cor,  Renes.

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.

Ask Doctor Section

Consult your doctor if you are lactose intolerant.

Pregnancy Or Breast Feeding Section

If you are pregnant or nursing, consult a doctor before use.

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