Pleo ® San STAPH 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 02:03:21

Label at a glance#

ProductPleo San Staph

Active ingredientstaphylococcus aureus

Label structure8 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Homeopathic Medicine

0.34 fl oz
(10 mL)

Indications

INDICATIONS & USAGE SECTION

For temporary relief of acne, boils & abscesses.

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTION

10 mL Staphylococcus aureus 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

1–2 × daily 5–10 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 - 10 mL Bottle Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Pleo^® San
STAPH
DROPS 6X

Homeopathic
Medicine

The original
SANUM^®
brand remedies

Indications: For
temporary relief
of acne, boils &
abscesses.

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
60681-1284-1	2019-11-13	C162847	48780-1	97449f38-c59c-f6ea-e053-dbdaa90aa703	Pleo ® San STAPH DROPS 6X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
60681-1284-1	Pleo San Staph	10 mL in 1 BOTTLE, DROPPER	SOLUTION/ DROPS	10		2
60681-1284-1	Pleo San Staph	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
60681-1284	PLEO SAN STAPH (STAPHYLOCOCCUS AUREUS) SOLUTION/ DROPS [SANUM KEHLBECK GMBH & CO. KG]	2	Legacy NDC, 2 package rows	20111115_1608a96f-add7-4447-a389-829300911633.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
staphylococcus aureus	ACTIVE INGREDIENT	O478WX4004	2
staphylococcus aureus	ACTIVE MOIETY	O478WX4004	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 San Staph
staphylococcus aureus
water

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
60681-1284	60681-1284-1

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
staphylococcus aureus	O478WX4004	ACTIB
water	059QF0KO0R	IACT

Source Document#

Source XML · Source PDF

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
c773add7-9d3c-4637-9e5d-650d15149748			1608a96f-add7-4447-a389-829300911633	2011-11-11	Warnings	Exact identifier spl id: c773add7-9d3c-4637-9e5d-650d15149748 spl set id: 1608a96f-add7-4447-a389-829300911633

Reported adverse events (FAERS/openFDA)#

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