MUCORSAN- mucor racemosus liquid

Country: United States

Language: English

Source: NLM (National Library of Medicine)

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Active ingredient:

MUCOR RACEMOSUS (UNII: 17RH99LQ7G) (MUCOR RACEMOSUS - UNII:17RH99LQ7G)

Available from:

sanPharma GmbH

Administration route:

ORAL

Prescription type:

OTC DRUG

Therapeutic indications:

For treatment of circulatory symptoms and blood-related conditions.

Authorization status:

unapproved homeopathic

Summary of Product characteristics

                                MUCORSAN- MUCOR RACEMOSUS 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._
----------
MUCORSAN
INDICATIONS
For treatment of circulatory symptoms and blood-related conditions.
DOS AGE
5-10 drops, three times daily.
INGREDIENTS
10ml Mucor racemosus 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
bioresource2@prodigy.net
DISTRIBUTED BY:
BioResource Inc.
Cotati CA 94931
PRINCIPAL DISPLAY PANEL - 10 ML BOTTLE CARTON
MucorSAN
Homeopathic
Medicine
For blood circulation
symptoms
0.34 FL OZ
(10ml)
sanPharma
biological health solutions
sanPharma GmbH
MUCORSAN
mucor racemosus liquid
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:6 4232-0 10
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
MUCO R RACEMO SUS (UNII: 17RH9 9 LQ7G) (MUCOR RACEMOSUS - UNII:17RH9 9
LQ7G)
MUCOR RACEMOSUS 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 10 -
0 3
1 in 1 CARTON
0 1/0 9 /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 v
                                
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