Storage and handling
protect from light and heat once opened do not use for more than 2 weeks
MucorSAN Oral Drops
- Manufacturer
- sanPharmacy Inc. | MEDsan Inc.
- Effective date
- 2024-04-25
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:26:48
Label at a glance#
ProductMucorSAN
Active ingredientMUCOR RACEMOSUS
Label structure9 sections
Contacts and useful links#
Label contents#
Full prescribing information#
Indications
For symptoms of circulatory disorders
OTC - PURPOSE SECTION
Relieves symptoms of circulatory disorders and other blood related conditions
Dosage
drop 5-10 drops into the mouth, three times daily
Warinings
If pregnant or breast-feeding, ask a health professional before use.
______________________________
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.
______________________________
When using this product
▪ do not use more than directed
______________________________
If symptoms persist more than 5 days, contact a licensed practitioner.
______________________________
Tamper Evident: Do not use product if tamper evident strip is broken. To report adverse events, contact MEDsan Inc. at 1-855-462-6334.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222
Ingredients
Mucor racemosus 4X
INACTIVE INGREDIENT SECTION
purified water, 0.09 g sodium chloride, 0.01 g potassium sorbate
Warnings
If pregnant or breast-feeding, ask a health professional before use.
______________________________
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.
______________________________
When using this product
▪ do not use more than directed
______________________________
If symptoms persist more than 5 days, contact a licensed practitioner.
______________________________
Tamper Evident: Do not use product if tamper evident strip is broken. To report adverse events, contact MEDsan Inc. at 1-855-462-6334.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222
SPL UNCLASSIFIED SECTION
Manufactured in the USA for:
sanPharmacy Inc.
350 Fifth Avenue STE 5220
New York NY 10118-5220
Liability statement
These statements or claims are based upon traditional homeopathic practice. They have not been reviewed by the Food & Drug Administration
STORAGE AND HANDLING SECTION
protect from light and heat
once opened do not use for more than 2 weeks
Principal Display Panel
MucorSAN
Homeopathic Medicine
For symptoms of circulatory disorders
Oral Drops
0.34 FL OZ (10 ml)
sanPharmacy
biological health solutions
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 73479-023-04 | 2025-07-29 | C162847 | 48780-1 | 3b156c62-2f10-fb37-e063-e6dba90a4e07 | MucorSAN Oral Drops |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73479-023-04 | MucorSAN | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | 1 | |
| 73479-023-04 | MucorSAN | 10 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 10 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- MucorSAN
- MUCOR RACEMOSUS
- WATER
- SODIUM CHLORIDE
- POTASSIUM SORBATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 73479-023 | 73479-023-04 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| POTASSIUM SORBATE | 1VPU26JZZ4 | IACT |
| MUCOR RACEMOSUS | 17RH99LQ7G | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 16ecc8da-dec5-a6e2-e063-6394a90ae249 | 16ecc8da-dec4-a6e2-e063-6394a90ae249 | 2024-04-25 | Warnings | 16ecc8da-dec5-a6e2-e063-6394a90ae249 16ecc8da-dec4-a6e2-e063-6394a90ae249 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.