Sucrose
FDA Label NDC 48951-9999

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 Sucrose (NDC 48951-9999). 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, keep out of reach of children, do not use section, ask doctor section, pregnancy or breast feeding section, questions section, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Purpose

Uses: Use according to standard homeopathic indications.

Dosage & Administration

Directions: Dissolve under the tongue 3-4 times daily. Age 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: ask a doctor.

Otc-Active Ingredient

Active Ingredient: Saccharum officinale (sucrose) 1X HPUS.

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.

Do Not Use Section

Warnings:  Do not use if allergic to any ingredient. Do not use if safety seal is broken or missing.

Ask Doctor Section

Consult a doctor if symptoms persist, if you are diabetic or intolerant of sugar.

Pregnancy Or Breast Feeding Section

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

Questions Section

Questions? Uriel Pharmacy

866 642-2858  East Troy, WI 53120 

www.urielpharmacy.com

NDC 48951-9999-2

Principal Display Panel

Sucrose

Homeopathic Pellets

net wt. 1 oz. (1350 pellets)

Sucrose Pellets Bottle Label (Sucp01)

Sucrose Pellets Bottle Label (Sucp01)


* Please review the disclaimer below.