ACONITUM BELLADONNA liquid

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H), APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z)

Available from:

Uriel Pharmacy Inc.

INN (International Name):

ATROPA BELLADONNA

Composition:

ATROPA BELLADONNA 4 [hp_X] in 1 mL

Administration route:

ORAL

Prescription type:

OTC DRUG

Therapeutic indications:

Directions: FOR ORAL USE. Use: Temporary relief of headache.

Authorization status:

unapproved homeopathic

Summary of Product characteristics

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
aconitum belladonna liquid
PRODUCT INFORMATION
Uriel Pharmacy Inc.
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:48951-9166
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF
STRENGTH
STRENGTH
ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA -
UNII:WQZ 3G9PF0H)
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
09/01/2009
1
1 mL in 1 AMPULE; Type 0: Not a Combination
Product
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: 11