MucorSAN by sanPharma GmbH MucorSAN

MucorSAN by

Drug Labeling and Warnings

MucorSAN by is a Homeopathic medication manufactured, distributed, or labeled by sanPharma GmbH. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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.

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MucorSAN

Indications

For treatment of circulatory symptoms and blood-related conditions.

Dosage

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

MUCORSAN 
mucor racemosus liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64232-010
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MUCOR RACEMOSUS (UNII: 17RH99LQ7G) (MUCOR RACEMOSUS - UNII:17RH99LQ7G)	MUCOR RACEMOSUS	4 [hp_X]  in 10 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64232-010-03	1 in 1 CARTON	01/09/2018
1		10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		01/09/2018	12/10/2019

Labeler - sanPharma GmbH (341409153)

Establishment
Name	Address	ID/FEI	Business Operations
sanPharma GmbH		341409153	manufacture(64232-010) , label(64232-010)

Revised: 12/2019

Document Id: 99584552-2a1b-4c4d-e053-2a95a90a288a

34390-5

Set id: 7efb1d66-3af5-4754-bd3d-e3e6ae1d0a6a

Version: 4

Effective Time: 20191210