Echinacea Argentum: Homeopathic Product Information

ECHINACEA ARGENTUM- echinacea, unspecified, silver, atropa belladonna and silicon dioxide liquid
Uriel Pharmacy Inc.

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Directions: FOR ORAL USE.

Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.

Active Ingredients: Echinacea e pl. tota (Purple coneflower) 3X, Atropa belladonna ex herba (Nightshade) 20X, Quartz (Rock crystal) 20X, Argentum met. (Silver) 30X

Inactive Ingredients: Water, Salt, Sodium bicarbonate, Rose oil

Use: Temporary relief of headache.

KEEP OUT OF REACH OF CHILDREN.

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.

REFRIGERATE AFTER OPENING. USE WITHIN 30 DAYS OF OPENING.
Opened on:_________________

Questions? Call 866.642.2858
Made by Uriel, East Troy, WI 53120
www.urielpharmacy.com Lot#

ECHINACEA ARGENTUM echinacea argentum liquid

Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-4166 Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ECHINACEA, UNSPECIFIED (ECHINACEA, UNSPECIFIED) ECHINACEA, UNSPECIFIED 3 [hp_X] in 1 mL SILVER (SILVER) SILVER 30 [hp_X] in 1 mL ATROPA BELLADONNA (ATROPA BELLADONNA) ATROPA BELLADONNA 20 [hp_X] in 1 mL SILICON DIOXIDE (SILICON DIOXIDE) SILICON DIOXIDE 20 [hp_X] in 1 mL

Inactive Ingredients Ingredient Name Strength WATER SODIUM CHLORIDE ROSE OIL SODIUM BICARBONATE

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:48951-4166-1 1 BOTTLE, DROPPER in 1 BAG contains a BOTTLE, DROPPER 1 10 mL in 1 BOTTLE, DROPPER This package is contained within the BAG (48951-4166-1)

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/01/2009

Labeler — Uriel Pharmacy Inc. (043471163)

Establishment
Name	Address	ID/FEI	Operations
Uriel Pharmacy Inc.		043471163	manufacture (48951-4166)

Revised: 05/2021 Uriel Pharmacy Inc.