Your browser does not support JavaScript! ACONITUM BELLADONNA LIQUID [URIEL PHARMACY INC.]
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ACONITUM BELLADONNA liquid
[Uriel Pharmacy Inc.]


Category DEA Schedule Marketing Status
HUMAN OTC DRUG LABEL unapproved homeopathic
NOTE: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.
Drug Label Sections

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 TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:48951-9166
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ATROPA BELLADONNA (ATROPA BELLADONNA) ATROPA BELLADONNA4 [hp_X]  in 1 mL
APIS MELLIFERA (APIS MELLIFERA) APIS MELLIFERA5 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM CHLORIDE 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48951-9166-110 in 1 BOX
11 mL in 1 AMPULE
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: 3/2014
 
Uriel Pharmacy Inc.

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