Pleo ® Lat DROPS 6X

Manufacturer
Sanum Kehlbeck GmbH & Co. KG
Effective date
2011-11-11
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:03:21

Label at a glance#

ProductPleo Lat
Active ingredientBACILLUS CEREUS
Label structure9 sections

Storage and handling

Protect from light and heat.

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Homeopathic Analgesic Medicine

Indications

INDICATIONS & USAGE SECTION

For temporary relief of muscle aches and pains.

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTION

5 mL Bacillus cereus 6X in a base of purified water.

Tamper Evident

OTC - DO NOT USE SECTION

Do not use this product if tamper-evident seal on base of bottle cap is missing or broken.

DOSAGE

DOSAGE & ADMINISTRATION SECTION

1–3 times 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 immediately.

STORAGE AND HANDLING SECTION

Protect from light and heat.

SPL UNCLASSIFIED SECTION

Made in Germany

Manufactured by:
SANUM-Kehlbeck
GmbH & Co. KG,
Hoya, Germany

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

Rev. 04/2010

PRINCIPAL DISPLAY PANEL - 5 mL Bottle Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Pleo® Lat
DROPS 6X

Homeopathic
Analgesic
Medicine

The original
SANUM®

brand remedies

Indications: For
temporary relief
of muscle aches and
pains.

0.17 fl oz
(5 mL)

Principal Display Panel - 5 mL Bottle Carton
Principal Display Panel - 5 mL Bottle Carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60681-1401-12019-11-13C16284748780-197449f38-d127-f6ea-e053-dbdaa90aa703Pleo ® Lat DROPS 6X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60681-1401-1Pleo Lat1 in 1 CARTONSOLUTION/ DROPS13
60681-1401-1Pleo Lat5 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS53

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60681-1401PLEO LAT (BACILLUS CEREUS) SOLUTION/ DROPS [SANUM KEHLBECK GMBH & CO. KG]3Legacy NDC, 2 package rows20111115_36438b22-a949-46fe-98d6-b3410a304f91.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BACILLUS CEREUSACTIVE INGREDIENT7YC151N82L3
BACILLUS CEREUSACTIVE MOIETY7YC151N82L3
waterINACTIVE INGREDIENT059QF0KO0R3

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60681-140160681-1401-1

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
NameUNIIKind
BACILLUS CEREUS7YC151N82LACTIB
water059QF0KO0RIACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
18279799-5076-4ae7-be08-f334fc893cd036438b22-a949-46fe-98d6-b3410a304f912011-11-11WarningsExact identifier
spl id: 18279799-5076-4ae7-be08-f334fc893cd0
spl set id: 36438b22-a949-46fe-98d6-b3410a304f91

Reported adverse events (FAERS/openFDA)#

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