ACONITUM BELLADONNA- aconitum belladonna 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.

----------

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 (Monkshood) 30X, Atropa belladonna (Nightshade) 30X, Rhus tox. (Sumac) 30X


Inactive Ingredients: Water, Salt

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.

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

Aconitum Belladonna Ampule

ACONITUM BELLADONNA 
aconitum belladonna liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-9166
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA4 [hp_X]  in 1 mL
APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z) APIS MELLIFERA5 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48951-9166-110 in 1 BOX09/01/2009
11 mL in 1 AMPULE; 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(48951-9166)

Revised: 11/2023
Document Id: 0995e648-9f31-9d3f-e063-6394a90ab072
Set id: 290883c6-0a6f-4a50-8895-4d5251b3c42e
Version: 5
Effective Time: 20231107
 
Uriel Pharmacy Inc.