MEDULLA OSSIUM 8 liquid

País: Estats Units

Idioma: anglès

Font: NLM (National Library of Medicine)

Compra'l ara

Descargar Fitxa tècnica (SPC)
16-01-2024

ingredients actius:

BOS TAURUS BONE MARROW (UNII: 08X0K2M57P) (BOS TAURUS BONE MARROW - UNII:08X0K2M57P)

Disponible des:

Uriel Pharmacy Inc.

Designació comuna internacional (DCI):

BOS TAURUS BONE MARROW

Composición:

BOS TAURUS BONE MARROW 8 [hp_X] in 1 mL

Vía de administración:

ORAL

tipo de receta:

OTC DRUG

indicaciones terapéuticas:

Directions: FOR ORAL USE. Use: Promotes healthy balance of homologous organs.

Estat d'Autorització:

unapproved homeopathic

Fitxa tècnica

                                MEDULLA OSSIUM 8- MEDULLA OSSIUM 8 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._
----------
MEDULLA OSSIUM 8
Directions: FOR ORAL USE.
Take the contents of one ampule under the tongue and hold for 30
seconds, then
swallow.
Active Ingredient: Medulla ossium (Bovine bone marrow) 8X
Inactive Ingredients: Water, Salt
"prepared using rhythmical processes"
Use: Promotes healthy balance of homologous organs.
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
MEDULLA OSSIUM 8
medulla ossium 8 liquid
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:48951-7023
ROUTE OF ADMINISTRATION
ORAL
Uriel Pharmacy Inc.
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF
STRENGTH
STRENGTH
BOS TAURUS BONE MARROW (UNII: 08X0K2M57P) (BOS TAURUS BONE
MARROW - UNII:08X0K2M57P)
BOS TAURUS BONE
MARROW
8 [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-
7023-1
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(48951-7023)
Revised: 1/2024
                                
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