Pleo™ –Lari DROPS 5X

Manufacturer: Sanum Kehlbeck GmbH & Co. KG
Effective date: 2011-08-01
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 02:03:16

Label at a glance#

ProductPleo Lari

Active ingredientlaricifomes officinalis fruiting body

Label structure10 sections

Storage and handling

Protect from light and heat.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Homeopathic Analgesic Medicine

0.34 fl oz
(10 mL)

Indications

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

For temporary relief of primary chronic polyarthritis symptoms.

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

10 mL Laricifomes officinalis e mycelio 5X.

INACTIVE INGREDIENT SECTION

Purified Water

Tamper Evident

OTC - DO NOT USE SECTION

Use this product only if tamper-evident strip at base of bottle cap is intact.

DOSAGE

DOSAGE & ADMINISTRATION SECTION

5–10 drops, once daily, before mealtime.

WARNING

WARNINGS SECTION

If symptoms persist more than a few days, contact a licensed practitioner. As with any other drugs, 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 other medications out of the reach of children. In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediately.

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. 02/2003

PRINCIPAL DISPLAY PANEL - 10 mL Bottle Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Pleo™ –Lari
DROPS 5X
Homeopathic
Analgesic
Medicine

Indications: For
temporary relief
of primary
chronic
polyarthritis
symptoms.

0.34 fl oz
(10 mL)

Principal Display Panel - 10 mL Bottle Carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
60681-1301-1	2019-10-29	C162847	48780-1	960f7f55-daf3-8e05-e053-dbdaa90a074a	Pleo™ –Lari DROPS 5X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
60681-1301-1	Pleo Lari	10 mL in 1 BOTTLE, DROPPER	SOLUTION/ DROPS	10		2
60681-1301-1	Pleo Lari	1 in 1 CARTON	SOLUTION/ DROPS	1		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
60681-1301	PLEO LARI (LARICIFOMES OFFICINALIS FRUITING BODY) SOLUTION/ DROPS [SANUM KEHLBECK GMBH & CO. KG]	2	Legacy NDC, 2 package rows	20110816_1bea81e9-bbcd-4cb1-8535-55a5b06b7ae8.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
laricifomes officinalis fruiting body	ACTIVE INGREDIENT	7IFM8431X3	2
laricifomes officinalis fruiting body	ACTIVE MOIETY	7IFM8431X3	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 Lari
laricifomes officinalis fruiting body
water

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
60681-1301	60681-1301-1

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
laricifomes officinalis fruiting body	7IFM8431X3	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
47f56433-ea33-4cb6-b6fd-8283d2302936			1bea81e9-bbcd-4cb1-8535-55a5b06b7ae8	2011-08-01	Warnings	Exact identifier spl id: 47f56433-ea33-4cb6-b6fd-8283d2302936 spl set id: 1bea81e9-bbcd-4cb1-8535-55a5b06b7ae8

Reported adverse events (FAERS/openFDA)#

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