ANTIMONIUM CRUDUM tablet

País: Estados Unidos

Idioma: inglés

Fuente: NLM (National Library of Medicine)

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Ficha técnica Ficha técnica (SPC)
30-12-2015

Ingredientes activos:

ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY TRISULFIDE - UNII:F79059A38U)

Disponible desde:

Rxhomeo Private Limited d.b.a. Rxhomeo, Inc

Designación común internacional (DCI):

ANTIMONY TRISULFIDE

Composición:

ANTIMONY TRISULFIDE 3 [hp_X]

Vía de administración:

ORAL

tipo de receta:

OTC DRUG

indicaciones terapéuticas:

Irritability, Eczema, Warts Condition listed above or as directed by the physician.

Estado de Autorización:

unapproved homeopathic

Ficha técnica

                                ANTIMONIUM CRUDUM- ANTIMONIUM CRUDUM TABLET
RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, 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._
----------
ACTIVE INGREDIENT
ANTIMONIUM CRUDUM HPUS 3X and Higher
USES
Irritability, Eczema, Warts
INDICATIONS
Condition listed above or as directed by the physician.
DOSAGE
Adults- Take 4 or 6 Tablets by mouth, three times daily or as
suggested by physician. Children 2 years
and older- take 1/2 the adult dose.
WARNINGS
This product is to be used for self-limiting conditions
If symptoms do not improve in 4 days, or worsen, discontinue use and
seek assistance of health
professional
As with any drug, if you are pregnant, or nursing a baby, seek
professional advice before taking this
product
Keep this and all medication out of reach of children
Do not use if capseal is broken or missing.
Close the cap tightly after use.
INACTIVE INGREDIENTS
Lactose
STORAGE
Store in a cool dark place
QUESTIONS OR COMMENTS
www.Rxhomeo.com | 1.888.2796642 | info@rxhomeo.com
Rxhomeo, Inc 9415 Burnet Road, Suite 312, Austin, TX 78758
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
ANTIMONIUM CRUDUM
antimonium crudum tablet
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:156 31-0 513
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
ANTIMO NY TRISULFIDE (UNII: F79 0 59 A38 U) (ANTIMONY TRISULFIDE -
UNII:F79 0 59 A38 U)
ANTIMONY TRISULFIDE 3 [hp_X]
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
LACTO SE (UNII: J2B2A4N9 8 G)
PRODUCT CHARACTERISTICS
COLOR
white
S CORE
no sco re
S HAP E
ROUND
S IZ E
3mm
FLAVOR
IMPRINT CODE
CONTAINS
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START DATE MARKETING END DATE
1
NDC:156 31-0 513-
0
1 in 1 BLISTER PACK; Type 0 : No t a Co mbinatio n Pro duct
2
NDC:156 31-0 513-1 4 in 1 BLISTER PACK; Type 0 : No t a Co mbinatio n
Pro duct
3
NDC:156 31-0 
                                
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