MucorSAN

Manufacturer
sanPharma GmbH
Effective date
2019-09-09
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 00:13:07

Label at a glance#

ProductMucorSAN
Active ingredientMUCOR RACEMOSUS
Label structure8 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Mucor racemosus 3X in amphiphilic cream base.

Indication

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

Wound healing, Hemorrhoids, Swellings, Contusions.

No preservatives added.

Ingredients

OTC - ACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTION

100g contain: 10g Active ingredient-dilution (Mucor racemosus 3X according to HAB regulation 5a with purified water); Inacitve ingredients: 35g Purified Water, 22,31g Petrolatum, 11,25g Propylene Glycol, 6,56g Caprylic/Capric Triglyceride, 6,13g PEG-20 Glyceryl Stearate, 5,25g Cetyl Alcohol, 3,5g Glyceryl Monostearate 60.

Dosage

DOSAGE & ADMINISTRATION SECTION

Apply sparsely to the affected area 3× daily unless otherwise indicated by your practitioner.

For external use only.

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. 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 - 150 ml Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

mucorSAN cream

wound-healing

sanPharma ®
biological health solutions

PRINCIPAL DISPLAY PANEL - 150 ml Bottle Label
PRINCIPAL DISPLAY PANEL - 150 ml Bottle Label

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64232-10264232-102-17

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
921dd6ec-dadf-4bf2-e053-2a95a90a85faa2dc4aaf-b0a8-48d5-a4dc-74bfb8431e282019-09-09WarningsExact identifier
spl id: 921dd6ec-dadf-4bf2-e053-2a95a90a85fa
spl set id: a2dc4aaf-b0a8-48d5-a4dc-74bfb8431e28

Reported adverse events (FAERS/openFDA)#

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