LEVICO PRUNUS- levico prunus 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.

----------

Levico Prunus

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: Hematite (Red iron ore) 3X, Hypericum (St. John’s Wort) 3X, Levico water (Mineral spring water) 3X, Prunus (Blackthorn) 3X

Inactive Ingredient: Organic sucrose

"prepared using rhythmical processes"

Use: Temporary relief of tiredness and fatigue.

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 shopuriel.com Lot:

Levico Prunus Pellet

LEVICO PRUNUS 
levico prunus pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-6027
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FERRIC OXIDE RED (UNII: 1K09F3G675) (FERRIC OXIDE RED - UNII:1K09F3G675) FERRIC OXIDE RED3 [hp_X]
ST. JOHN'S WORT (UNII: UFH8805FKA) (ST. JOHN'S WORT - UNII:UFH8805FKA) ST. JOHN'S WORT3 [hp_X]
FERROUS ARSENATE (UNII: 129CO35H12) (FERROUS ARSENATE - UNII:129CO35H12) FERROUS ARSENATE3 [hp_X]
SLOE (UNII: 3MLB4858X7) (SLOE - UNII:3MLB4858X7) SLOE3 [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:48951-6027-21350 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(48951-6027)

Revised: 2/2024
Document Id: 1068265e-c8d6-d57d-e063-6294a90af35e
Set id: 27d6fdad-2c7a-4582-ba46-71dad4dd8d0a
Version: 4
Effective Time: 20240202
 
Uriel Pharmacy Inc.