ACONITUM BELLADONNA- atropa belladonna and apis mellifera 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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Aconitum Belladonna

Directions: FOR ORAL USE.

Take the contents of one ampule
under the tongue and hold for
30 seconds, then swallow.

Active Ingredients: Aconitum
e tub. 30X, Atropa belladonna
e rad. 30X, Rhus tox. e fol. 30X


Inactive Ingredients: Water, Salt

Use: Temporary relief of headache.

KEEP OUT OF REACH OF CHILDREN.

Warnings: 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. Natural ingredients may cause color, scent
and/or taste variation.

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

product label

ACONITUM BELLADONNA 
aconitum belladonna liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-9166
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA 4 [hp_X]  in 1 mL
APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z) APIS MELLIFERA 5 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:48951-9166-1 10 in 1 BOX
1 1 mL in 1 AMPULE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 09/01/2009
Labeler - Uriel Pharmacy Inc. (043471163)
Establishment
Name Address ID/FEI Business Operations
Uriel Pharmacy Inc. 043471163 manufacture(48951-9166)

Revised: 3/2014
Document Id: df250aba-48bd-4cd4-bfd0-57caf21b1df8
Set id: 290883c6-0a6f-4a50-8895-4d5251b3c42e
Version: 1
Effective Time: 20140320
 
Uriel Pharmacy Inc.