PLEO MUC- mucor racemosus liquid

Pleo Muc by

Drug Labeling and Warnings

Pleo Muc by is a Homeopathic medication manufactured, distributed, or labeled by Sanum Kehlbeck GmbH & Co KG. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Homeopathic Ophthalmic Demulcent Medicine without preservatives

Indications

For temporary relief of irritated and dry eyes

Active Ingredient per 0.017 fl oz / 0.5 ml vial

0.05 mg Mucor racemosus

Inactive ingredient

water, salt

Tamper Evident

Do not use this product if tamper-evident aluminum foil is missing or broken.

DOSAGE

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

WARNING

If symptoms persist, contact a licensed practitioner.

Do not touch tip of container to any surface.

Keep this and all other medications out of the reach of children. In case of ingestion, get professional help or contact a Poison Control Center.

If you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours, discontinue use and consult a doctor.

Do not use if solution changes color or becomes cloudy. The vials are for single use only and should be discarded after that use.

SPL UNCLASSIFIED SECTION

Distributed by:
SANUM USA Corp.
1465 Slater Road
Ferndale, WA 98248

Manufactured by:
Sanum-Kehlbeck
GmbH & Co. KG

PRINCIPAL DISPLAY PANEL - 5 ml Carton

Pleo® Muc EYE DROPS 5X

10 Single use vials

Homeopathic Ophthalmic Demulcent Medicine
without preservatives

Indications: For temporary relief of
irritated and dry eyes

The original
SANUM®
brand remedies

0.17 fl oz / 5 ml (10 x 0.017 fl oz / 0.5 ml vials)

INGREDIENTS AND APPEARANCE

PLEO MUC 
mucor racemosus liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60681-1822
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
mucor racemosus (UNII: 17RH99LQ7G) (mucor racemosus - UNII:17RH99LQ7G)	mucor racemosus	5 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
sodium chloride (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60681-1822-1	2 in 1 CARTON
1		5 in 1 POUCH
1		0.5 mL in 1 AMPULE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
UNAPPROVED HOMEOPATHIC		06/15/2011

Labeler - Sanum Kehlbeck GmbH & Co KG (318386133)

Establishment
Name	Address	ID/FEI	Business Operations
Sanum Kehlbeck GmbH & Co KG		318386133	MANUFACTURE