ACONITUM BELLADONNA

Main information

  • Trade name:
  • ACONITUM BELLADONNA- aconitum belladonna liquid
  • Composition:
  • ATROPA BELLADONNA 4 [hp_X] in 1 mL
  • Administration route:
  • ORAL
  • Prescription type:
  • OTC DRUG
  • Medicine domain:
  • Humans
  • Medicine type:
  • Homeopathic medication

Documents

Localization

  • Available in:
  • ACONITUM BELLADONNA- aconitum belladonna liquid
    United States
  • Language:
  • English

Therapeutic information

  • Therapeutic indications:
  • Directions: FOR ORAL USE. Use: Temporary relief of headache.

Status

  • Source:
  • DailyMed - NLM - National Library of Medicine
  • Authorization status:
  • unapproved homeopathic
  • Authorization number:
  • 48951-9166-1
  • Last update:
  • 24-06-2019

Summary of Product characteristics: dosage, interactions, side effects

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.

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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 (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

www.urielpharmacy.com

ACONITUM BELLADONNA

aconitum belladonna liquid

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:48 9 51-9 16 6

Route of Administration

ORAL

Uriel Pharmacy Inc.

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

ATRO PA BELLADO NNA (UNII: WQZ3G9 PF0 H) (ATROPA BELLADONNA -

UNII:WQZ3G9 PF0 H)

ATROPA

BELLADONNA

4 [hp_X]

in 1 mL

APIS MELLIFERA (UNII: 7S8 2P3R43Z) (APIS MELLIFERA - UNII:7S8 2P3R43Z)

APIS MELLIFERA

5 [hp_X]

in 1 mL

Inactive Ingredients

Ingredient Name

Stre ng th

WATER (UNII: 0 59 QF0 KO0 R)

SO DIUM CHLO RIDE (UNII: 451W47IQ8 X)

Packag ing

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

1

NDC:48 9 51-9 16 6 -1

10 in 1 BOX

0 9 /0 1/20 0 9

1

1 mL in 1 AMPULE; Type 0 : No t a Co mbinatio n Pro duct

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

unappro ved ho meo pathic

0 9 /0 1/20 0 9

Labeler -

Uriel Pharmacy Inc. (043471163)

Establishment

Name

Ad d re s s

ID/FEI

Busine ss Ope rations

Uriel Pharmacy Inc.

0 4347116 3

ma nufa c ture (48 9 51-9 16 6 )

Revised: 4/2018