BELLADONNA BETULA FORMICA- belladonna betula formica liquid 
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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Belladonna Betula Formica

Directions: FOR ORAL USE.

Active Ingredients: Betula e fol. (Silver Birch leaves) 3X, Atropa belladonna ex herba (Nightshade) 6X, Formica ex animale (Red wood ant) 6X

Inactive Ingredients: Water, Salt, Boric acid, Sodium bicarbonate, Rose oil

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. 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.

REFRIGERATE AFTER OPENING. USE WITHIN 30 DAYS OF OPENING.
Opened on:_________________

Questions? Call 866.642.2858
Made by Uriel, East Troy, WI 53120
www.urielpharmacy.com

Belladonna Betula FormicaBelladonna Betula Formica 10ml

BELLADONNA BETULA FORMICA 
belladonna betula formica liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-2133
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA6 [hp_X]  in 1 mL
FORMICA RUFA (UNII: 55H0W83JO5) (FORMICA RUFA - UNII:55H0W83JO5) FORMICA RUFA6 [hp_X]  in 1 mL
BETULA PENDULA LEAF (UNII: 5HW39H9KDH) (BETULA PENDULA LEAF - UNII:5HW39H9KDH) BETULA PENDULA LEAF3 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
BORIC ACID (UNII: R57ZHV85D4)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
ROSE OIL (UNII: WUB68Y35M7)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48951-2133-11 in 1 BAG09/01/2009
110 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
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(48951-2133)

Revised: 9/2019
Document Id: 92aec9ba-4322-ecdd-e053-2995a90a6c23
Set id: 92aec9ba-4321-ecdd-e053-2995a90a6c23
Version: 1
Effective Time: 20190916
 
Uriel Pharmacy Inc.