CACTUS CRATAEGUS- cactus crataegus 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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Cactus Crataegus

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: Cactus ex herba (Queen of the night) 3X, Crataegus e fol. et fruct. (Hawthorn) 3X, Melissa ex herba (Lemon balm) 3X

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

CactusCrataegusPellets

CACTUS CRATAEGUS 
cactus crataegus pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-3005
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SELENICEREUS GRANDIFLORUS STEM (UNII: 7114SV0MYK) (SELENICEREUS GRANDIFLORUS STEM - UNII:7114SV0MYK) SELENICEREUS GRANDIFLORUS STEM3 [hp_X]
HAWTHORN LEAF WITH FLOWER (UNII: 6OM09RPY36) (HAWTHORN LEAF WITH FLOWER - UNII:6OM09RPY36) HAWTHORN LEAF WITH FLOWER3 [hp_X]
MELISSA OFFICINALIS (UNII: YF70189L0N) (MELISSA OFFICINALIS - UNII:YF70189L0N) MELISSA OFFICINALIS3 [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:48951-3005-21350 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(48951-3005)

Revised: 6/2018
Document Id: 6d97e1e0-ba1a-0610-e053-2a91aa0af072
Set id: 0b83ea9d-0c6e-4042-ae29-ed9d51c92233
Version: 3
Effective Time: 20180601
 
Uriel Pharmacy Inc.