Pleo Sanuvis

Product NDC
60681-6301
11-digit product format
606816301
Labeler code
60681
Product ID
60681-6301_3d49e515-0833-4585-bcbd-e8382a0bb006
Type
HUMAN OTC DRUG
Nonproprietary name
lactic acid, l-
Dosage form
OINTMENT
Route
TOPICAL
Labeler
Sanum Kehlbeck GmbH & Co. KG
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2010-06-15
Marketing end
0000-00-00
Substance
LACTIC ACID, L-
Active strength
1 [hp_X]/30g
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60681-6301-12019-10-21C16284748780-1956f9ecf-cdef-621f-e053-dbdaa90a74adPleo ® Sanuvis Ointment 1X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60681-6301-1Pleo Sanuvis1 in 1 CARTONOINTMENT11
60681-6301-1Pleo Sanuvis30 g in 1 TUBEOINTMENT301

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60681-6301PLEO SANUVIS (LACTIC ACID, L-) OINTMENT [SANUM KEHLBECK GMBH & CO. KG]1Legacy NDC, 2 package rows20100702_3c8d0d4f-d94e-4bd7-adba-788378da6847.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
60681-6301-1606816301011 in 1 CARTONHistorical