Nail MD

Product NDC
55992-711
11-digit product format
559920711
Labeler code
55992
Product ID
55992-711_10c85210-171d-4786-bac7-29ff0e86a4cc
Type
HUMAN OTC DRUG
Nonproprietary name
Miconazole Nitrate
Dosage form
CREAM
Route
TOPICAL
Labeler
OMG Medical Group, LLC
Application
part333C
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2013-02-14
Marketing end
0000-00-00
Substance
MICONAZOLE NITRATE
Active strength
200 mg/mg
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3a55f4fb-5aec-4c88-0ff7-4d608ad4866aProduct name120140508
5b9a7965-36d2-8412-dcaf-f76a65411611Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55992-711-012019-11-27C16284748780-19855e2a2-3648-60a7-e053-dbdaa90a05bdNail MD

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55992-711-01Nail MD200 mg in 1 PACKAGECREAM2007

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55992-711NAIL MD (MICONAZOLE NITRATE) CREAM [OMG MEDICAL GROUP, LLC]7Legacy NDC, 1 package rows20131217_bf425745-09db-4290-9329-b1760051c93e.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
55992-711-0155992071101200 mg in 1 PACKAGE200 mgHistorical