PETASITES VERONICA- petasites veronica 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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Petasites Veronica

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: Abies (White fir ) 3X, Petasites (Butterbur) 3X, Veronica (Speedwell) 3X, Plantago (Ribwort plantain) 4X

Inactive Ingredient: Organic sucrose

Use: Temporary relief of cough.

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. 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

shopuriel.com Lot:

Petasites Quercus Pellets

PETASITES VERONICA 
petasites veronica pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-8022
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ABIES ALBA LEAFY TWIG (UNII: CE3G3J56LR) (ABIES ALBA LEAFY TWIG - UNII:CE3G3J56LR) ABIES ALBA LEAFY TWIG3 [hp_X]
PETASITES HYBRIDUS ROOT (UNII: 97S2809V5R) (PETASITES HYBRIDUS ROOT - UNII:97S2809V5R) PETASITES HYBRIDUS ROOT3 [hp_X]
VERONICA OFFICINALIS FLOWERING TOP (UNII: 9IH82J936J) (VERONICA OFFICINALIS FLOWERING TOP - UNII:9IH82J936J) VERONICA OFFICINALIS FLOWERING TOP3 [hp_X]
PLANTAGO MAJOR LEAF (UNII: 7DC28K241X) (PLANTAGO MAJOR LEAF - UNII:7DC28K241X) PLANTAGO MAJOR 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:48951-8022-21350 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(48951-8022)

Revised: 10/2023
Document Id: 08f1c9dd-6224-2250-e063-6294a90ac875
Set id: 588f6bf4-739a-418a-9065-596812d9239c
Version: 4
Effective Time: 20231030
 
Uriel Pharmacy Inc.