Pleo ® Poly Om DROPS 9X

Manufacturer
Sanum Kehlbeck GmbH & Co. KG
Effective date
2010-10-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:02:41

Label at a glance#

ProductPleo Poly Om
Active ingredientlactococcus lactis immunoserum rabbit, streptococcus pyogenes immunoserum rabbit, streptococcus viridans group immunoserum rabbit, staphylococcus epidermidis immunoserum rabbit, staphylococcus aureus immunoserum rabbit, streptococcus pneumoniae immunoserum rabbit, mycobacterium bovis immunoserum rabbit
Label structure10 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Homeopathic Medicine

0.34 fl oz
(10 mL)

Indications

INDICATIONS & USAGE SECTION

skin conditions, such as warts and moles.

DOSAGE

DOSAGE & ADMINISTRATION SECTION

Unless otherwise prescribed, apply 5-10 drops into the bend of the elbow and rub in three times daily.

WARNING

WARNINGS SECTION

OTC - ASK DOCTOR SECTION

If symptoms persist more than a few days, contact a licensed practitioner.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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 other medications out of the reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

OTC - WHEN USING SECTION

Protect from light and heat.

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

10 mL aqueous dilution contains: antitoxins and antigens 9X of Streptococcus lacticus, -pyogenes, -haemolyticus, - viridans; Staphylococcus albus, -pharyngis, -aureus; Diplococcus lanceolatus; Mycobacterium tuberculosis typus bovinus.

INACTIVE INGREDIENT SECTION

Inactive Ingredient water

Tamper Evident

OTC - DO NOT USE SECTION

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

SPL UNCLASSIFIED SECTION

Made in Germany

SPL UNCLASSIFIED SECTION

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

SPL UNCLASSIFIED SECTION

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

Rev. 05/2010

PRINCIPAL DISPLAY PANEL - 10 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Pleo® Poly Om DROPS 9X (applied topically)

Homeopathic Medicine

Indications: skin conditions, such as warts and moles.

0.34 fl oz (10 mL)

Dosage: Unless otherwise prescribed, 5-10 drops into the bend of the elbow and rub in three
times daily. Warning: 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. 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. Protect from light and heat. TAMPER EVIDENT: Do not use this
product if tamper-evident seal on base of bottle cap is missing or broken. INGREDIENTS: 10 mL
aqueous dilution contains: antitoxins and antigens 9X of Streptococcus lacticus, -pyogenes,
-haemolyticus, -viridans; Staphylococcus albus, -pharyngis, -aureus; Diplococcus lanceolatus;
Mycobacterium tuberculosis typus bovinus.
Rev. 05/2010

Principal Display Panel - 10 mL Bottle Label
Principal Display Panel - 10 mL Bottle Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60681-2808-12019-10-29C16284748780-1960f7f55-d3d3-8e05-e053-dbdaa90a074aPleo ® Poly Om DROPS 9X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60681-2808-1Pleo Poly Om1 in 1 CARTONSOLUTION/ DROPS11
60681-2808-1Pleo Poly Om10 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60681-2808PLEO POLY OM (LACTOCOCCUS LACTIS IMMUNOSERUM RABBIT, STREPTOCOCCUS PYOGENES IMMUNOSERUM RABBIT, STREPTOCOCCUS VIRIDANS GROUP IMMUNOSERUM RABBIT, STAPHYLOCOCCUS EPIDERMIDIS IMMUNOSERUM RABBIT, STAPHYLOCOCCUS AUREUS IMMUNOSERUM RABBIT, STREPTOCOCCUS PNEUMONIAE IMMUNOSERUM RABBIT, AND MYCOBACTERIUM BOVIS IMMUNOSERUM RABBIT) SOLUTION/ DROPS [SANUM KEHLBECK GMBH & CO. KG]1Legacy NDC, 2 package rows20101023_68835302-9345-413f-b843-88ec4541e9aa.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
lactococcus lactis immunoserum rabbitACTIVE INGREDIENTAST1Y049U11
mycobacterium bovis immunoserum rabbitACTIVE INGREDIENTNNW4543CRP1
staphylococcus aureus immunoserum rabbitACTIVE INGREDIENTQ1G8TGQ05J1
staphylococcus epidermidis immunoserum rabbitACTIVE INGREDIENT8409DJA34Y1
streptococcus pneumoniae immunoserum rabbitACTIVE INGREDIENTIWJ46H2H5C1
streptococcus pyogenes immunoserum rabbitACTIVE INGREDIENT726RS6QMS81
streptococcus viridans group immunoserum rabbitACTIVE INGREDIENT4U4OEA495W1
lactococcus lactis immunoserum rabbitACTIVE MOIETYAST1Y049U11
mycobacterium bovis immunoserum rabbitACTIVE MOIETYNNW4543CRP1
staphylococcus aureus immunoserum rabbitACTIVE MOIETYQ1G8TGQ05J1
staphylococcus epidermidis immunoserum rabbitACTIVE MOIETY8409DJA34Y1
streptococcus pneumoniae immunoserum rabbitACTIVE MOIETYIWJ46H2H5C1
streptococcus pyogenes immunoserum rabbitACTIVE MOIETY726RS6QMS81
streptococcus viridans group immunoserum rabbitACTIVE MOIETY4U4OEA495W1
waterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60681-280860681-2808-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

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
bb2c59f0-e661-46e7-a137-09cee6b48b5068835302-9345-413f-b843-88ec4541e9aa2010-10-08WarningsExact identifier
spl id: bb2c59f0-e661-46e7-a137-09cee6b48b50
spl set id: 68835302-9345-413f-b843-88ec4541e9aa

Reported adverse events (FAERS/openFDA)#

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