Pleo ® Sanuvis Ointment 1X

Manufacturer: Sanum Kehlbeck GmbH & Co. KG
Effective date: 2010-06-04
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:02:21

Label at a glance#

ProductPleo Sanuvis

Active ingredientlactic acid, l-

Label structure8 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

for topical use only

Homeopathic External Analgesic Medicine

1.05 oz (30g)

Indications

INDICATIONS & USAGE SECTION

For temporary relief of pain of bruises, sprains, swelling of joints and muscles.

DOSAGE

DOSAGE & ADMINISTRATION SECTION

Apply thinly on the affected area 1-3 times daily.

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 other 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 fom light and heat.

Tamper Evident

OTC - DO NOT USE SECTION

Do not use this product if metal seal under the tube cap is missing or broken.

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

SPL UNCLASSIFIED SECTION

1g ointment contains: 0.1g Acidum L(+) - lacticum 1X.

Inactive ingredients

INACTIVE INGREDIENT SECTION

lanolin alcohol, glycerylmonostearate, propylene glycol, polyglyceryl-3, cocoate magnesium sulfate, water.

SPL UNCLASSIFIED SECTION

Made in Germany

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

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

Rev. 03/2010

PRINCIPAL DISPLAY PANEL - 30g Tube Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Pleo^® Sanuvis
Ointment 1X

for topical use only

Homeopathic
External Analgesic
Medicine

The original
SANUM ^®
brand remedies

Indications: For temporary
relief of pain of bruises,
sprains, swelling of joints
and muscles.

1.05 oz (30g)

Principal Display Panel - 30g Tube Carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
60681-6301-1	2019-10-21	C162847	48780-1	956f9ecf-cdef-621f-e053-dbdaa90a74ad	Pleo ® Sanuvis Ointment 1X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
60681-6301-1	Pleo Sanuvis	1 in 1 CARTON	OINTMENT	1		1
60681-6301-1	Pleo Sanuvis	30 g in 1 TUBE	OINTMENT	30		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
60681-6301	PLEO SANUVIS (LACTIC ACID, L-) OINTMENT [SANUM KEHLBECK GMBH & CO. KG]	1	Legacy NDC, 2 package rows	20100702_3c8d0d4f-d94e-4bd7-adba-788378da6847.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
lactic acid, l-	ACTIVE INGREDIENT	F9S9FFU82N	1
lactic acid, l-	ACTIVE MOIETY	F9S9FFU82N	1
glyceryl monostearate	INACTIVE INGREDIENT	230OU9XXE4	1
lanolin alcohols	INACTIVE INGREDIENT	884C3FA9HE	1
water	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

Pleo Sanuvis
lactic acid, l-
glyceryl monostearate
lanolin alcohols
water

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
60681-6301	60681-6301-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
lactic acid, l-	F9S9FFU82N	ACTIB
glyceryl monostearate	230OU9XXE4	IACT
lanolin alcohols	884C3FA9HE	IACT
water	059QF0KO0R	IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 25 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
lanolin alcohols	LANOLIN ALCOHOLS	884C3FA9HE	CREAM / TOPICAL	6 %w/w		Exact identifier — unii candidate 4 equally ranked IID candidates
lanolin alcohols	LANOLIN ALCOHOLS	884C3FA9HE	OINTMENT / TOPICAL		452 mg	Exact identifier — unii candidate 4 equally ranked IID candidates
glyceryl monostearate	GLYCERYL MONOSTEARATE	230OU9XXE4	LOTION / TOPICAL		177 mg	Exact identifier — unii candidate 21 equally ranked IID candidates
glyceryl monostearate	GLYCERYL MONOSTEARATE	230OU9XXE4	TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE / ORAL		23 mg	Exact identifier — unii candidate 21 equally ranked IID candidates
glyceryl monostearate	GLYCERYL MONOSTEARATE	230OU9XXE4	CAPSULE / ORAL	13.75 mg		Exact identifier — unii candidate 21 equally ranked IID candidates
glyceryl monostearate	GLYCERYL MONOSTEARATE	230OU9XXE4	TABLET / SUBLINGUAL	1.23 mg		Exact identifier — unii candidate 21 equally ranked IID candidates
glyceryl monostearate	GLYCERYL MONOSTEARATE	230OU9XXE4	TABLET, DELAYED RELEASE / ORAL		6 mg	Exact identifier — unii candidate 21 equally ranked IID candidates
glyceryl monostearate	GLYCERYL MONOSTEARATE	230OU9XXE4	GRANULE, FOR SUSPENSION / ORAL		4 mg	Exact identifier — unii candidate 21 equally ranked IID candidates
glyceryl monostearate	GLYCERYL MONOSTEARATE	230OU9XXE4	AEROSOL, FOAM / VAGINAL	3 %w/w		Exact identifier — unii candidate 21 equally ranked IID candidates
glyceryl monostearate	GLYCERYL MONOSTEARATE	230OU9XXE4	SUSPENSION / OPHTHALMIC	0.5 %w/v		Exact identifier — unii candidate 21 equally ranked IID candidates
glyceryl monostearate	GLYCERYL MONOSTEARATE	230OU9XXE4	OINTMENT / TOPICAL	5 %w/w		Exact identifier — unii candidate 21 equally ranked IID candidates
glyceryl monostearate	GLYCERYL MONOSTEARATE	230OU9XXE4	TABLET, CHEWABLE / ORAL		1 mg	Exact identifier — unii candidate 21 equally ranked IID candidates
glyceryl monostearate	GLYCERYL MONOSTEARATE	230OU9XXE4	CAPSULE, EXTENDED RELEASE / ORAL	32.4 mg		Exact identifier — unii candidate 21 equally ranked IID candidates
glyceryl monostearate	GLYCERYL MONOSTEARATE	230OU9XXE4	LIQUID / TOPICAL	1 %w/w		Exact identifier — unii candidate 21 equally ranked IID candidates
glyceryl monostearate	GLYCERYL MONOSTEARATE	230OU9XXE4	TABLET / ORAL	33.34 mg		Exact identifier — unii candidate 21 equally ranked IID candidates
glyceryl monostearate	GLYCERYL MONOSTEARATE	230OU9XXE4	EMULSION / ORAL	NA		Exact identifier — unii candidate 21 equally ranked IID candidates
glyceryl monostearate	GLYCERYL MONOSTEARATE	230OU9XXE4	SUPPOSITORY / RECTAL	35 mg		Exact identifier — unii candidate 21 equally ranked IID candidates
glyceryl monostearate	GLYCERYL MONOSTEARATE	230OU9XXE4	CREAM / VAGINAL		140 mg	Exact identifier — unii candidate 21 equally ranked IID candidates
lanolin alcohols	LANOLIN ALCOHOLS	884C3FA9HE	OINTMENT / OPHTHALMIC	10 %w/w		Exact identifier — unii candidate 4 equally ranked IID candidates
glyceryl monostearate	GLYCERYL MONOSTEARATE	230OU9XXE4	AEROSOL, FOAM / TOPICAL	3.27 %w/w		Exact identifier — unii candidate 21 equally ranked IID candidates
glyceryl monostearate	GLYCERYL MONOSTEARATE	230OU9XXE4	CAPSULE, DELAYED RELEASE / ORAL		15 mg	Exact identifier — unii candidate 21 equally ranked IID candidates
lanolin alcohols	LANOLIN ALCOHOLS	884C3FA9HE	LOTION / TOPICAL		9360 mg	Exact identifier — unii candidate 4 equally ranked IID candidates
glyceryl monostearate	GLYCERYL MONOSTEARATE	230OU9XXE4	SUSPENSION / AURICULAR (OTIC)	0.5 %w/v		Exact identifier — unii candidate 21 equally ranked IID candidates
glyceryl monostearate	GLYCERYL MONOSTEARATE	230OU9XXE4	CREAM / TOPICAL		836 mg	Exact identifier — unii candidate 21 equally ranked IID candidates
glyceryl monostearate	GLYCERYL MONOSTEARATE	230OU9XXE4	TABLET, EXTENDED RELEASE / ORAL		529 mg	Exact identifier — unii candidate 21 equally ranked IID candidates

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
3d49e515-0833-4585-bcbd-e8382a0bb006			3c8d0d4f-d94e-4bd7-adba-788378da6847	2010-06-04	Warnings	Exact identifier spl id: 3d49e515-0833-4585-bcbd-e8382a0bb006 spl set id: 3c8d0d4f-d94e-4bd7-adba-788378da6847

Reported adverse events (FAERS/openFDA)#

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