BRYONIA STANNUM liquid

Country: United States

Language: English

Source: NLM (National Library of Medicine)

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Active ingredient:

BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B), TIN (UNII: 387GMG9FH5) (TIN - UNII:387GMG9FH5)

Available from:

Uriel Pharmacy Inc.

INN (International Name):

BRYONIA ALBA ROOT

Composition:

BRYONIA ALBA ROOT 3 [hp_X] in 1 mL

Administration route:

ORAL

Prescription type:

OTC DRUG

Therapeutic indications:

Directions: FOR ORAL USE. Use: Temporary relief of sore joints.

Authorization status:

unapproved homeopathic

Summary of Product characteristics

                                BRYONIA STANNUM- BRYONIA STANNUM 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._
----------
BRYONIA STANNUM
Directions: FOR ORAL USE.
Take the contents of one ampule under the tongue and hold for 30
seconds, then
swallow.
Active Ingredients: Bryonia (White bryony) 3X, Stannum met. (Metallic
tin) 17X
Inactive Ingredients: Water, Salt
"prepared using rhythmical processes"
Use: Temporary relief of sore joints.
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
Made by Uriel, East Troy, WI 53120
shopuriel.com
BRYONIA STANNUM
bryonia stannum liquid
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:48951-2086
ROUTE OF ADMINISTRATION
ORAL
Uriel Pharmacy Inc.
ROUTE OF ADMINISTRATION
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF
STRENGTH
STRENGTH
BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT -
UNII:T7J046YI2B)
BRYONIA ALBA ROOT
3 [hp_X] in 1 mL
TIN (UNII: 387GMG9FH5) (TIN - UNII:387GMG9FH5)
TIN
17 [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-
2086-1
10 in 1 BOX
09/01/2009
1
1 mL in 1 AMPULE; Type 1: Convenience Kit of Co-
Package
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(48951-2086)
Revised: 1/
                                
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