MucorSAN

Label at a glance#

Label contents#

Full prescribing information#

Indications

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

For treatment of circulatory symptoms and blood-related conditions.

Dosage

DOSAGE & ADMINISTRATION SECTION

5-10 drops, three times daily.

Ingredients

OTC - ACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTION

10ml Mucor racemosus 4X in a base of purified water, 0.09g sodium chloride, 0.01g potassium sorbate.

Warning

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medications out of the reach of children. Protect from light and heat.

Tamper Evident

SPL UNCLASSIFIED SECTION

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

SPL UNCLASSIFIED SECTION

Distributed By:
BioResource Inc.
Cotati CA 94931

PRINCIPAL DISPLAY PANEL - 10 ml Bottle Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MucorSAN

Homeopathic
Medicine

For blood circulation
symptoms

0.34 FL OZ
(10ml)

sanPharma
biological health solutions

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

• MucorSAN
• MUCOR RACEMOSUS
• WATER
• SODIUM CHLORIDE
• POTASSIUM SORBATE

NDC Codes#

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.