Ferrum Silicicum Urtica: Homeopathic Product Information

FERRUM SILICICUM URTICA- anise, urtica dioica, silicon dioxide and ferric oxide red 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 the contents of one ampule under the tongue and hold for 30 seconds, then swallow.

Active Ingredient: Anisum (Anise) 4X, Urtica dioica (Stinging nettle) 3X, Ferrum sesquioxide (Iron oxide) 6X, Nontronite — Ferrum silic. (Nat. Iron silicate) 6X

Inactive Ingredients: Water, Salt, Lactose

Use: Temporary relief of headache.

KEEP OUT OF REACH OF CHILDREN.

Warnings: Claims based on traditional homepoathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Contains traces of lactose. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use.

Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
shopuriel.com

Lot:

FERRUM SILICICUM URTICA ferrum silicicum urtica liquid

Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-4173 Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANISE (ANISE) ANISE 4 [hp_X] in 1 mL URTICA DIOICA (URTICA DIOICA) URTICA DIOICA 3 [hp_X] in 1 mL SILICON DIOXIDE (SILICON DIOXIDE) SILICON DIOXIDE 6 [hp_X] in 1 mL FERRIC OXIDE RED (FERRIC OXIDE RED) FERRIC OXIDE RED 6 [hp_X] in 1 mL

Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE WATER LACTOSE, UNSPECIFIED FORM

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:48951-4173-1 10 AMPULE in 1 BOX contains a AMPULE 1 1 mL in 1 AMPULE This package is contained within the BOX (48951-4173-1)

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 (48951-4173)

Revised: 09/2023 Uriel Pharmacy Inc.