ROQUEFOSAN- penicillium roqueforti liquid

País: Estados Unidos

Língua: inglês

Origem: NLM (National Library of Medicine)

Ingredientes ativos:

PENICILLIUM ROQUEFORTI (UNII: 7ORP6R724L) (PENICILLIUM ROQUEFORTI - UNII:7ORP6R724L)

Disponível em:

sanPharma GmbH

Via de administração:

ORAL

Tipo de prescrição:

OTC DRUG

Indicações terapêuticas:

For intestinal symptoms.

Status de autorização:

unapproved homeopathic

Características técnicas

ROQUEFOSAN- PENICILLIUM ROQUEFORTI LIQUID
SANPHARMA GMBH
_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._
----------
ROQUEFOSAN
INDICATIONS
For intestinal symptoms.
DOS AGE
5-10 drops, three times daily.
INGREDIENTS
10ml Penicillium roqueforti 4X in a base of purified water, 0.09g
sodium chloride, 0.01g potassium
sorbate.
WARNING
If symptoms persist more than a few days, contact a licensed
practitioner. As with any drug, if you are
pregnant or nursing a baby, seek the advice of a health care
professional before using this product.
Keep this and all medications out of the reach of children.
Protect from light and heat.
TAMPER EVIDENT
Do not use product if tamper evident strip is broken or removed from
base of cap. To report adverse
events, contact BioResource at 707/664-9023 or
[e-mail]
DISTRIBUTED BY:
BioResource Inc.
Cotati CA 94931
PRINCIPAL DISPLAY PANEL - 10 ML BOTTLE CARTON
ROQUEFOSAN
Homeopathic
Medicine
For intestinal
symptoms
0.34 FL OZ
(10ML)
san PHARMA
biological health solutions
sanPharma GmbH
ROQUEFOSAN
penicillium roqueforti liquid
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:6 4232-0 35
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
PENICILLIUM RO Q UEFO RTI (UNII: 7ORP6 R724L) (PENICILLIUM ROQUEFORTI
-
UNII:7ORP6 R724L)
PENICILLIUM
ROQUEFORTI
4 [hp_X]
in 10 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WATER (UNII: 0 59 QF0 KO0 R)
SO DIUM CHLO RIDE (UNII: 451W47IQ8 X)
PO TASSIUM SO RBATE (UNII: 1VPU26 JZZ4)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:6 4232-0 35-
18
1 in 1 CARTON
0 2/0 1/20 18
1
10 mL in 1 BOTTLE, DROPPER; Type 0 : No t a Co mbinatio n
Pro duc t
MARKETING INFORMATION
MARKE TING CATE GORY
APPLICATION NUMBE R OR MONOGRAPH CITATION
MARKE TING START DATE
MARKE TING END DATE
unappro ved