SOLANUM NIGRUM pellet

Land: Vereinigte Staaten

Sprache: Englisch

Quelle: NLM (National Library of Medicine)

Wirkstoff:

SOLANUM NIGRUM WHOLE (UNII: 0FMD6WV47M) (SOLANUM NIGRUM WHOLE - UNII:0FMD6WV47M)

Verfügbar ab:

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

Verabreichungsweg:

ORAL

Verschreibungstyp:

OTC DRUG

Anwendungsgebiete:

Nightmares Condition listed above or as directed by the physician

Berechtigungsstatus:

unapproved homeopathic

Fachinformation

SOLANUM NIGRUM- SOLANUM NIGRUM PELLET
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
SOLANUM NIGRUM HPUS 3X and higher
USES
Nightmares
INDICATIONS
Condition listed above or as directed by the physician
DOSAGE
Adults- Take 4 or 6 Pellets 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
Sucrose
STORAGE
Store in a cool dark place
QUESTIONS OR COMMENTS
www.Rxhomeo.com | 1.888.2796642 | [e-mail]
Rxhomeo, Inc 9415 Burnet Road, Suite 312, Austin, TX 78758
SOLANUM NIGRUM
solanum nigrum pellet
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:156 31-0 40 7
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
SO LANUM NIGRUM WHO LE (UNII: 0 FMD6 WV47M) (SOLANUM NIGRUM WHOLE -
UNII:0 FMD6 WV47M)
SOLANUM NIGRUM
WHOLE
3 [hp_X]
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
SUCRO SE (UNII: C151H8 M554)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START DATE
MARKETING END DATE
1
NDC:156 31-0 40 7-0
10 0 in 1 PACKAGE; Type 0 : No t a Co mbinatio n Pro duct
0 1/0 1/20 18
2
NDC:156 31-0 40 7-1
20 0 in 1 PACKAGE; Type 0 : No t a Co mbinatio n Pro duct
0 1/0 1/20 18
3
NDC:156 31-0 40 7-2
40 0 in 1 PACKAGE; Type 0 : No t a Co mbinatio n Pro duct
0 1/0 1/20 18
4
NDC:156 31-0 40 7-3
750 in 1 PACKAGE; Type 0 : No t a Co mbinatio n Pr