Pleo™ San CAND DROPS 6X

Manufacturer: Sanum-Kehlbeck GmbH & Co. KG
Effective date: 2012-03-07
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 02:03:34

Label at a glance#

ProductPleo San Cand

Active ingredientcandida albicans

Label structure9 sections

Storage and handling

Protect from light and heat.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Homeopathic Medicine

Indications

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

For temporary relief of sore mouth and gums.

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTION

10 mL Candida albicans 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

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

Manufactured By:
Sanum-Kehlbeck,
GmbH & Co. KG

Rev. 06/2005

PRINCIPAL DISPLAY PANEL - 10 mL Bottle, Dropper Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Pleo^® San
CAND
DROPS 6X

Homeopathic
Medicine

The original
SANUM ^®
brand remedies

lndications: For
temporary relief
of sore mouth
and gums.

0.34 fl oz
(10 mL)

PRINCIPAL DISPLAY PANEL - 10 mL Bottle, Dropper Carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
60681-1316-1	2019-11-13	C162847	48780-1	97449f38-becd-f6ea-e053-dbdaa90aa703	Pleo™ San CAND DROPS 6X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
60681-1316-1	Pleo San Cand	10 mL in 1 BOTTLE, DROPPER	SOLUTION/ DROPS	10		2
60681-1316-1	Pleo San Cand	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
60681-1316	PLEO SAN CAND (CANDIDA ALBICANS) SOLUTION/ DROPS [SANUM-KEHLBECK GMBH & CO. KG]	2	Legacy NDC, 2 package rows	20120313_0eb43466-bc82-4838-baf6-b8e5df740e6a.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
candida albicans	ACTIVE INGREDIENT	4D7G21HDBC	2
candida albicans	ACTIVE MOIETY	4D7G21HDBC	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 Cand
candida albicans
water

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
60681-1316	60681-1316-1

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
candida albicans	4D7G21HDBC	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
3e382f17-20e5-4eb7-b6a3-8e4915220aea			0eb43466-bc82-4838-baf6-b8e5df740e6a	2012-03-07	Warnings	Exact identifier spl id: 3e382f17-20e5-4eb7-b6a3-8e4915220aea spl set id: 0eb43466-bc82-4838-baf6-b8e5df740e6a

Reported adverse events (FAERS/openFDA)#

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