ONOPORDON COMP.- onopordon comp. 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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Onopordon comp.

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: 100gm contains: 25gm Onopordon (Cotton thistle) 1X, 25gm Primula (Cowslip) 1X, 25gm Hyoscyamus (Henbane) 4X

Inactive Ingredient: Organic sucrose

Use: Promotes healthy circulatory support.

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

OnopordonCompPellets

ONOPORDON COMP. 
onopordon comp. pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-7090
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ONOPORDUM ACANTHIUM FLOWER (UNII: AP97AUF88E) (ONOPORDUM ACANTHIUM FLOWER - UNII:AP97AUF88E) ONOPORDUM ACANTHIUM FLOWER1 [hp_X]
PRIMULA VERIS FLOWER (UNII: W5BET37294) (PRIMULA VERIS FLOWER - UNII:W5BET37294) PRIMULA VERIS FLOWER1 [hp_X]
HYOSCYAMUS NIGER LEAF (UNII: 32IT7G8BAW) (HYOSCYAMUS NIGER LEAF - UNII:32IT7G8BAW) HYOSCYAMUS NIGER LEAF4 [hp_X]
Inactive Ingredients
Ingredient NameStrength
SUCROSE (UNII: C151H8M554)  
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize3mm
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48951-7090-21350 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 Inc.043471163manufacture(48951-7090)

Revised: 6/2018
Document Id: 6de986ff-0b83-f4cc-e053-2991aa0a160e
Set id: 54f0716d-4eb8-4330-a83b-7b4b86ba5b44
Version: 3
Effective Time: 20180605
 
Uriel Pharmacy Inc.