Miconazole Nitrate

Product NDC
41250-575
11-digit product format
412500575
Labeler code
41250
Product ID
41250-575_21b29ec4-99e6-31cf-e063-6394a90aeb2e
Type
HUMAN OTC DRUG
Nonproprietary name
Anti-fungal Powder Miconazole Nitrate Talc Free
Dosage form
POWDER
Route
TOPICAL
Labeler
Meijer Distribution Inc
Application
M005
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2017-12-01
Marketing end
2026-05-31
Substance
MICONAZOLE NITRATE
Active strength
1.42 g/71g
Pharmacologic classes
Azole Antifungal [EPC], Azoles [CS]
NDC exclude flag
No
Current FDA listing
Yes

DailyMed Product Concepts#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41250-575-25Miconazole Nitrate71 g in 1 BOTTLE, PLASTICPOWDER7110

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41250-575MICONAZOLE NITRATE (ANTI-FUNGAL POWDER MICONAZOLE NITRATE TALC FREE) POWDER [MEIJER DISTRIBUTION INC]10Current NDC, Legacy NDC, 1 package rows20240910_0c795360-d385-4e2f-a3bb-5ad3bad1fa2c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
41250-575-254125005752571 g in 1 BOTTLE, PLASTIC (41250-575-25) 71 g2017-12-012026-05-31NoNoCurrent