Melissa Chamomilla
FDA Label NDC 48951-7152

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 Melissa Chamomilla (NDC 48951-7152). 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 section, ask doctor section, pregnancy or breast feeding section, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Purpose

Uses: Temporarily relieves symptoms of menopausal complaints, such as hot flashes, nerves, sleeplessness or nervous irritability.

Dosage & Administration

Directions: Dissolve under tongue 3 times daily, or up to every hour. Age 12 and older: 10 pellets. Under age 12: ask a doctor.

Inactive Ingredient

Inactive Ingredients: Sucrose, Bryophyllum e fol. 3X, Sepia e secreto 6X.

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.

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 48951-7029-2

* Please review the disclaimer below.