Pleo Usti

Product NDC
60681-5604
11-digit product format
606815604
Labeler code
60681
Product ID
60681-5604_c720aca5-a43e-47d2-8928-ed6182ba5e5c
Type
HUMAN OTC DRUG
Nonproprietary name
ustilago maydis
Dosage form
SUPPOSITORY
Route
RECTAL
Labeler
Sanum Kehlbeck GmbH & Co. KG
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2004-04-21
Marketing end
0000-00-00
Substance
USTILAGO MAYDIS
Active strength
5 [HP_X]/1
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
60681-5604-12019-10-21C16284748780-1956f9ecf-d7ee-621f-e053-dbdaa90a74adPleo™ Usti SUPPOSITORIES 5X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60681-5604-1Pleo Usti10 in 1 DOSE PACKSUPPOSITORY101
60681-5604-1Pleo Usti1 in 1 CARTONSUPPOSITORY11

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ustilago maydisACTIVE INGREDIENT4K7Z7K7SWGPLEO USTI (USTILAGO MAYDIS) SUPPOSITORY [SANUM KEHLBECK GMBH & CO. KG]1
ustilago maydisACTIVE MOIETY4K7Z7K7SWGPLEO USTI (USTILAGO MAYDIS) SUPPOSITORY [SANUM KEHLBECK GMBH & CO. KG]1
lactoseINACTIVE INGREDIENTJ2B2A4N98GPLEO USTI (USTILAGO MAYDIS) SUPPOSITORY [SANUM KEHLBECK GMBH & CO. KG]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60681-5604PLEO USTI (USTILAGO MAYDIS) SUPPOSITORY [SANUM KEHLBECK GMBH & CO. KG]1Legacy NDC, 2 package rows20110113_8e5065f8-7281-43fc-936a-80c04a52ae6c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
60681-5604-16068156040110 in 1 DOSE PACKHistorical