Miconazole Nitrate

Product NDC
30142-840
11-digit product format
301420840
Labeler code
30142
Product ID
30142-840_2900d8d7-ecfa-6aae-e063-6294a90a9000
Type
HUMAN OTC DRUG
Nonproprietary name
Anti-fungal Powder Miconazole Nitrate Talc Free
Dosage form
POWDER
Route
TOPICAL
Labeler
Kroger Co.
Application
M005
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-04-11
Marketing end
2026-05-30
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
30142-840-01Miconazole Nitrate71 g in 1 BOTTLE, PLASTICPOWDER716

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
30142-840MICONAZOLE NITRATE (ANTI-FUNGAL POWDER MICONAZOLE NITRATE TALC FREE) POWDER [KROGER CO.]6Current NDC, Legacy NDC, 1 package rows20241213_dc75579c-3daf-00d7-e053-2a95a90a88a9.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
30142-840-013014208400171 g in 1 BOTTLE, PLASTIC (30142-840-01) 71 g2022-04-122026-05-30NoNoCurrent