Pleo ® San SALM DROPS 6X

Manufacturer
Sanum Kehlbeck GmbH & Co. KG
Effective date
2011-11-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:03:22

Label at a glance#

ProductPleo San Salm
Active ingredientsalmonella enterica subsp. enterica serovar enteritidis
Label structure9 sections

Storage and handling

Protect from light and heat.

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Homeopathic Medicine

0.34 fl oz
(10 mL)

Indications

INDICATIONS & USAGE SECTION

For loss of appetite.

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTION

10 mL Salmonella enteritidis 6X in a base of purified water.

Tamper Evident

OTC - DO NOT USE SECTION

Do not use this product if tamper evident seal at base of bottle cap is missing or broken or if imprinted security strip on carton is torn.

DOSAGE

DOSAGE & ADMINISTRATION SECTION

1–2 x daily 5–10 drops.

WARNING

WARNINGS SECTION

If symptoms persist more than a few days, contact a licensed practitioner. As with any other 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. 03/2010

PRINCIPAL DISPLAY PANEL - 10 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Pleo® San
SALM
DROPS 6X

Homeopathic
Medicine

The original
SANUM®
brand remedies

Indications: For
loss of appetite.

0.34 fl oz
(10 mL)

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
60681-1264-12019-11-13C16284748780-197449f38-b8a9-f6ea-e053-dbdaa90aa703Pleo ® San SALM DROPS 6X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60681-1264-1Pleo San Salm1 in 1 CARTONSOLUTION/ DROPS12
60681-1264-1Pleo San Salm10 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS102

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60681-1264PLEO SAN SALM (SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS) SOLUTION/ DROPS [SANUM KEHLBECK GMBH & CO. KG]2Legacy NDC, 2 package rows20111115_eca6f1e4-d093-4d33-871b-654587e3c823.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
salmonella enterica subsp. enterica serovar enteritidisACTIVE INGREDIENTY3V16D4PV42
salmonella enterica subsp. enterica serovar enteritidisACTIVE MOIETYY3V16D4PV42
waterINACTIVE INGREDIENT059QF0KO0R2

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
60681-126460681-1264-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 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
47d611f2-e495-4774-b0b3-acd9dd826a8feca6f1e4-d093-4d33-871b-654587e3c8232011-11-11WarningsExact identifier
spl id: 47d611f2-e495-4774-b0b3-acd9dd826a8f
spl set id: eca6f1e4-d093-4d33-871b-654587e3c823

Reported adverse events (FAERS/openFDA)#

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