FERRUM SILICICUM URTICA- ferrum silicicum urtica pellet
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.

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Ferrum silicicum Urtica

Directions: FOR ORAL USE ONLY.

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

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

Inactive Ingredient: Organic sucrose

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. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. 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.

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

FerrumSilicicumUrticaPellets

FERRUM SILICICUM URTICA
ferrum silicicum urtica pellet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:48951-4075
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ANISE (UNII: 21C2F5E8RE) (ANISE - UNII:21C2F5E8RE)	ANISE	3 [hp_X]
URTICA DIOICA ROOT (UNII: J8HE8A6E5T) (URTICA DIOICA ROOT - UNII:J8HE8A6E5T)	URTICA DIOICA ROOT	3 [hp_X]
FERRIC OXIDE RED (UNII: 1K09F3G675) (FERRIC OXIDE RED - UNII:1K09F3G675)	FERRIC OXIDE RED	6 [hp_X]
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	6 [hp_X]

Ingredient Name	Strength
Inactive Ingredients
SUCROSE (UNII: C151H8M554)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	3mm
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:48951-4075-2	1350 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	09/01/2009	11/06/2023

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		09/01/2009	11/06/2023

Labeler - Uriel Pharmacy Inc. (043471163)

Name	Address	ID/FEI	Business Operations
Establishment
Uriel Pharmacy Inc.		043471163	manufacture(48951-4075)

Revised: 11/2023

Document Id: 09935a74-34b1-0e7c-e063-6294a90a7c83

Set id: fc251b53-7615-4327-a15c-e41e13fd704d

Version: 4

Effective Time: 20231107

Uriel Pharmacy Inc.