Storage and handling
Protect from light and heat.
MUCOR DROPS 4X
- Manufacturer
- USPharmaCo | DermaMed
- Effective date
- 2009-12-23
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:02:06
Label at a glance#
ProductMucor
Active ingredientMucor racemosus
Label structure9 sections
Contacts and useful links#
Websitewww.uspharmaco.com
www.uspharmaco.com
www.uspharmaco.comLabel contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Homeopathic Medicine
Indications
For temporary relief of pain from bruises, sprains, and swelling of joints and muscles
Dosage
5-10. drops, three times daily.
Active Ingredient
Mucor racemosus 4X
Inactive Ingredients
Purified water, sodium chloride, 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, 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 reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
STORAGE AND HANDLING SECTION
Protect from light and heat.
Tamper Evident
Do not use product if the tamper evident strip is broken or removed from the base of the cap.
SPL UNCLASSIFIED SECTION
To report serious adverse events, call: 1-877-557-4276 or 1-623-582-3110
Manufactured for and distributed by:
USPharmaCo Distribution Ltd.
2205 W. Lone Cactus Drive #19,
Phoenix, AZ 85027www.uspharmaco.com
info@uspharmaco.com
Made in Canada
PRINCIPAL DISPLAY PANEL - 10 ml Label
MUCOR DROPS 4X
Homeopathic Medicine 0.34 fl. oz. (10ml)
Indications: For temporary relief of pain from bruises, sprains, and swelling of joints and muscles
Dosage: 5-10 drops, three times daily.
Active Ingredient: Mucor racemosus 4X
Inactive Ingredients: Purified water, sodium chloride, 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, seek the advice of a health care professional before
using this product. Keep this and all medications out of reach of children. In case of overdose,
get medical help or contact a Poison Control Center right away.Protect from light and heat.
Tamper Evident: Do not use product if the tamper evident strip is broken or removed from the
base of the cap.
To report serious adverse events, call: 1-877-557-4276 or 1-623-582-3110
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 49693-1301-1 | 2019-10-21 | C162847 | 48780-1 | 956f9ecf-cc24-621f-e053-dbdaa90a74ad | MUCOR DROPS 4X |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 49693-1301-1 | Mucor | 10 mL in 1 BOTTLE | LIQUID | 10 | 1 | |
| 49693-1301-1 | Mucor | 1 in 1 BOX | LIQUID | 1 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 49693-1301 | MUCOR (MUCOR RACEMOSUS) LIQUID [USPHARMACO] | 1 | Legacy NDC, 2 package rows | 20091228_e9f31592-ec62-48b6-b12b-503b8ad81d78.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Mucor racemosus | ACTIVE INGREDIENT | 17RH99LQ7G | 1 | |
| Mucor racemosus | ACTIVE MOIETY | 17RH99LQ7G | 1 |
Products#
Every source-derived product name is available through these pages.
- Mucor
- Mucor racemosus
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 49693-1301 | 49693-1301-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| 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 |
|---|---|---|---|---|---|---|
| 87f66e2e-ffef-400b-bf7a-cfff9d99e14a | e9f31592-ec62-48b6-b12b-503b8ad81d78 | 2009-12-23 | Warnings | 87f66e2e-ffef-400b-bf7a-cfff9d99e14a e9f31592-ec62-48b6-b12b-503b8ad81d78 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.