GELSEMIUM BRYONIA- gelsemium bryonia 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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Gelsemium Bryonia

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: Bryonia (White bryony) 3X, Gelsemium (Yellow jasmine) 3X, Vivianite (Nat. ferrous phosphate) 7X

Inactive Ingredients: Organic sucrose,
Lactose

Use: Temporary relief of flu symptoms.

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. Contains traces of lactose. 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

GelsemiumBryoniaPellets

GELSEMIUM BRYONIA 
gelsemium bryonia pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-5097
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (GELSEMIUM SEMPERVIRENS ROOT - UNII:639KR60Q1Q) GELSEMIUM SEMPERVIRENS ROOT3 [hp_X]
BRYONIA CRETICA SUBSP. DIOICA ROOT (UNII: 53UB5FH7CX) (BRYONIA CRETICA SUBSP. DIOICA ROOT - UNII:53UB5FH7CX) BRYONIA CRETICA SUBSP. DIOICA ROOT3 [hp_X]
Inactive Ingredients
Ingredient NameStrength
LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
SUCROSE (UNII: C151H8M554)  
Product Characteristics
Colorwhite (white) Scoreno score
ShapeROUND (round) Size3mm
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48951-5097-21350 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product09/01/2009
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic09/01/2009
Labeler - Uriel Pharmacy Inc (043471163)
Establishment
NameAddressID/FEIBusiness Operations
Uriel Pharmacy Inc043471163manufacture(48951-5097)

Revised: 6/2018
Document Id: 6dd5153f-0e04-bb2b-e053-2a91aa0aa291
Set id: 6b2e26a7-ed61-4252-8043-bd546a4f3f09
Version: 3
Effective Time: 20180604
 
Uriel Pharmacy Inc