MUCOR EYE DROPS 5X

Manufacturer: USPharmaCo | DermaMed
Effective date: 2009-12-21
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 02:02:09

Label at a glance#

ProductMucor

Active ingredientMucor racemosus

Label structure10 sections

Storage and handling

Protect from light and heat.

Contacts and useful links#

PhoneLabel contact1-623-582-3110

Websitewww.uspharmaco.com

www.uspharmaco.com

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Homeopathic Medicine

Indications

INDICATIONS & USAGE SECTION

For temporary relief of dry, itching, or burning eyes due to allergic or other irritating factors

Dosage

DOSAGE & ADMINISTRATION SECTION

1 drop twice daily, into affected eye(s).

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Mucor racemosus 5X

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Isotonic sodium chloride solution, chlorhexidine diacetate.

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, 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

OTC - DO NOT USE SECTION

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: 1-623-582-3110

Manufactured for and distributed by:
USPharmaCo Distribution Ltd.
2205 W. Lone Cactus Drive #19,
Phoenix, AZ 85027
www.uspharmaco.com
info@uspharmaco.com

Made in Canada

PRINCIPAL DISPLAY PANEL - 5 mL Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MUCOR EYE DROPS 5X

Homeopathic Medicine 0.17 fl. oz. (5ml)

Indications: For temporary relief of dry, itching, or burning eyes due to allergic or other irriating factors
Dosage: 1 drop twice daily, into affected eye(s).
Active Ingredient: Mucor racemosus 5X
Inactive Ingredients: Isotonic sodium chloride solution, chlorhexidine diacetate.
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: 1-623-582-3110

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
49693-1306-1	2019-10-21	C162847	48780-1	956f9ecf-dc9e-621f-e053-dbdaa90a74ad	MUCOR EYE DROPS 5X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
49693-1306-1	Mucor	5 mL in 1 BOTTLE	LIQUID	5		2
49693-1306-1	Mucor	1 in 1 BOX	LIQUID	1		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49693-1306	MUCOR (MUCOR RACEMOSUS) LIQUID [USPHARMACO]	2	Legacy NDC, 2 package rows	20100116_9023368b-eecd-458f-b332-84d0495dc94a.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
Mucor racemosus	ACTIVE INGREDIENT	17RH99LQ7G	2
Mucor racemosus	ACTIVE MOIETY	17RH99LQ7G	2

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

Mucor
Mucor racemosus

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
49693-1306	49693-1306-1

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
Mucor racemosus	17RH99LQ7G	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
bb64565a-3f29-4b46-be43-84373e03c67f			9023368b-eecd-458f-b332-84d0495dc94a	2009-12-21	Warnings	Exact identifier spl id: bb64565a-3f29-4b46-be43-84373e03c67f spl set id: 9023368b-eecd-458f-b332-84d0495dc94a

Reported adverse events (FAERS/openFDA)#

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