FDA.reportPublic FDA data

MucorSAN

Manufacturer
sanPharma GmbH
Effective date
2019-05-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:23:44

Label at a glance#

ProductMucorSAN
Active ingredientMUCOR RACEMOSUS
Label structure7 sections

Storage and handling

Protect from light and heat.

Label contents#

Full prescribing information#

Indications

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

For blood circulation symptoms

Dosage

DOSAGE & ADMINISTRATION SECTION

1-2 capsules per day, taken at least 1 hour before eating.

Ingredients

OTC - ACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTION

285mg Mucor racemosus 4X in a base of lactose and beet oil.

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.

STORAGE AND HANDLING SECTION

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

PRINCIPAL DISPLAY PANEL - 30 Capsule Can Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MucorSAN

Homeopathic Medicine

For blood circulation symptoms

30 Capsules

sanPharma
biological health solutions

Principal display Panel - MucorSAN CapsulesPrincipal display Panel - MucorSAN Capsules

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64232-01264232-012-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYPROMELLOSE, UNSPECIFIED3NXW29V3WOIACT
LACTOSE MONOHYDRATEEWQ57Q8I5XIACT
MUCOR RACEMOSUS17RH99LQ7GACTIB

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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
89787c61-0273-11b3-e053-2995a90af38c8977ef7d-41b5-c152-e053-2995a90a217c2019-05-22WarningsExact identifier
spl id: 89787c61-0273-11b3-e053-2995a90af38c
spl set id: 8977ef7d-41b5-c152-e053-2995a90a217c

Reported adverse events (FAERS/openFDA)#

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