Pleo™ Art "U" DROPS 6X

Manufacturer: Sanum Kehlbeck GmbH & Co. KG
Effective date: 2012-03-07
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 02:03:35

Label at a glance#

ProductPleo Art U

Active ingredientBrevibacterium Stationis

Label structure9 sections

Storage and handling

Protect from light and heat.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Homeopathic Medicine

0.34 fl oz
(10 mL)

Indications

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

To temporarily restore mental alertness during periods of fatigue

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTION

10 mL Corynebacterium sp. 6X in a base of purified water.

Tamper Evident

OTC - DO NOT USE SECTION

Do not use this product if the plastic band at base of bottle cup is broken.

DOSAGE

DOSAGE & ADMINISTRATION SECTION

1–3 × weekly 2–5 drops.

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. In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediataly.

STORAGE AND HANDLING SECTION

Protect from light and heat.

SPL UNCLASSIFIED SECTION

Made in Germany.

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

Manufactured By:
Sanum-Kehlbeck
GmbH & Co. KG

Rev. 8/2001

PRINCIPAL DISPLAY PANEL - 10 mL Bottle, Dropper Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Pleo^® Art
"U"
DROPS 6X

Homeopathic
Medicine

The original
SANUM^®
brand remedies

Indications: To
temporarily restore
mental alertness
during periods
of fatigue.

0.34 fl oz
(10 mL)

PRINCIPAL DISPLAY PANEL - 10 mL Bottle, Dropper Carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
60681-0401-1	2019-11-13	C162847	48780-1	97449f38-d34c-f6ea-e053-dbdaa90aa703	Pleo™ Art "U" DROPS 6X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
60681-0401-1	Pleo Art U	1 in 1 CARTON	SOLUTION/ DROPS	1		2
60681-0401-1	Pleo Art U	10 mL in 1 BOTTLE, DROPPER	SOLUTION/ DROPS	10		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
60681-0401	PLEO ART U (BREVIBACTERIUM STATIONIS) SOLUTION/ DROPS [SANUM KEHLBECK GMBH & CO. KG]	2	Legacy NDC, 2 package rows	20120313_be9343ef-d1cf-491c-ab18-cb1431d9bbf1.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
Brevibacterium Stationis	ACTIVE INGREDIENT	118V62TZ38	2
Brevibacterium Stationis	ACTIVE MOIETY	118V62TZ38	2
water	INACTIVE INGREDIENT	059QF0KO0R	2

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

Pleo Art U
Brevibacterium stationis
water

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
60681-0401	60681-0401-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
Brevibacterium Stationis	118V62TZ38	ACTIB
water	059QF0KO0R	IACT

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
af3ada15-2db9-4843-9f44-5ab428ac87aa			be9343ef-d1cf-491c-ab18-cb1431d9bbf1	2012-03-07	Warnings	Exact identifier spl id: af3ada15-2db9-4843-9f44-5ab428ac87aa spl set id: be9343ef-d1cf-491c-ab18-cb1431d9bbf1

Reported adverse events (FAERS/openFDA)#

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