NDC 51672-2001-01 - Miconazole Nitrate

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
51672-2001
Requested NDC
51672-2001-01
Package NDCs from labels
51672-2001-1, 51672-2001-2, 51672-2001-01
Manufacturer
Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc.
Effective date
2026-08-25
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Miconazole NitrateSun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc.2026-08-25HUMAN OTC DRUG LABEL
Miconazole Nitrate - A-S Medication SolutionsA-S Medication Solutions2025-12-03HUMAN OTC DRUG LABEL
Miconazole Nitrate - A-S Medication SolutionsA-S Medication Solutions2025-02-24HUMAN OTC DRUG LABEL
Miconazole NitrateNuCare Pharmaceuticals,Inc.2022-03-15HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51672-2001-1Miconazole Nitrate1 in 1 CARTONCREAM15
51672-2001-1Miconazole Nitrate15 g in 1 TUBECREAM155
51672-2001-2Miconazole Nitrate1 in 1 CARTONCREAM15
51672-2001-2Miconazole Nitrate30 g in 1 TUBECREAM305

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51672-2001MICONAZOLE NITRATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.]4Current NDC, Legacy NDC, 4 package rows20241222_7fd4037e-d350-47b7-a7d9-a43b8e366fa0.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51672-2001-1GM - Gram51672-20019dbd7e37-8219-4939-b49c-0359e914af9712012-07-24
51672-2001-2GM - Gram51672-20019cf50338-1157-450f-91bd-7c055b0d494812013-02-13

DailyMed Socrata Ingredients#

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 34 of 70 · 1,400 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Antifungal LiquidTOLNAFTATEVALU MERCHANDISERS, COf4abb499-6893-9efb-e053-2995a90a33ed2025-11-24WarningsExact identifier
application number: M005
TolnafateTOLNAFTATE ATHLETES FOOT POWDER SPRAY TALC FREEVALU MERCHANDISERS, CO9ac97d4a-169b-49ff-aa34-ccb5b43726a12025-11-24WarningsExact identifier
application number: M005
TolnafateFOOT ODOR CONTROL POWDER SPRAYVALU MERCHANDISERS, CO51b69b0f-d63f-4fe0-87e6-722f955687612025-11-24WarningsExact identifier
application number: M005
PUR-WASHWATERNiagara Pharmaceuticals Inc.beda35c3-9a8b-47ad-e053-2995a90a7b1b2025-11-24WarningsExact identifier
unii: 059QF0KO0R
Easy Care First Aid EyewashWATERTender Corporationa070aac8-e6d2-ef10-e053-2a95a90aa5b12025-11-24WarningsExact identifier
unii: 059QF0KO0R
PUR-WASHWATERNiagara Pharmaceuticals Inc.e07a064b-f680-405c-bbcd-24fac430951e2025-11-24WarningsExact identifier
unii: 059QF0KO0R
ULINE EyewashEYEWASHNiagara Pharmaceuticals Inc.2d7f22d2-320b-6af1-e063-6294a90addc62025-11-24WarningsExact identifier
unii: 059QF0KO0R
Pur-WashEYEWASHNiagara Pharmaceuticals, Inc.0d43b1c1-2699-37f1-e054-00144ff88e882025-11-24WarningsExact identifier
unii: 059QF0KO0R
PUR-WASHWATERNiagara Pharmaceuticals Inc.777e1559-786f-8d54-e053-2991aa0aa98d2025-11-24WarningsExact identifier
unii: 059QF0KO0R
PUR-WASHWATERNiagara Pharmaceuticals Inc.7289103a-5cbf-42f4-8848-e827149a43ca2025-11-24WarningsExact identifier
unii: 059QF0KO0R
Miconazole Nitrate Antifungal PowderMICONAZOLE NITRATE ANTIFUNGAL POWDERMarlex Pharmaceuticals, Inc.de4f703c-39e9-855e-e053-2a95a90a6ea92025-11-21WarningsExact identifier
application number: M005
unii: VW4H1CYW1K
Odor-Eaters Athletes FootTOLNAFTATEBlistex Inc.20d795d1-2345-4d4f-8439-07ad11ff8f652025-11-21WarningsExact identifier
application number: M005
Eyewash Additive ConcentrateWATER AND PROPYLENE GLYCOLHaws Corporationdd168403-398c-41ff-b1df-d93e4ff39de32025-11-20WarningsExact identifier
unii: 059QF0KO0R
Derman AntifungalZINC UNDECYLENATECompania Internacional de Comercio, S.A.P.I de C.V.0129d801-90f6-49fd-857f-27d6ba9fc66c2025-11-19WarningsExact identifier
application number: M005
ClotrimazoleCLOTRIMAZOLEA-S Medication Solutions9afb964c-9b88-4701-adcf-7070e25cb6c12025-11-19WarningsExact identifier
application number: M005
AU KAH CHUEN ANTIFUNGALCLOTRIMAZOLEANHUI DONGSHENGYOUBANG PHARMACEUTICAL CO., LTD.3a262bcd-e6c0-4554-ab1c-9c861f90e1902025-11-18WarningsExact identifier
application number: M005
Sterile WaterWATERFresenius Kabi USA, LLCfd823bef-c14c-4708-a18a-8aaa8470412f2025-11-18Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Cura Hongo AntifungalCLOTRIMAZOLEPharmadel LLCdf031309-2778-00cf-e053-2a95a90a5eea2025-11-17WarningsExact identifier
application number: M005
CharmTex All in One Antibacterial Shave Gel Body WashBENZETHONIUM CHLORIDELiufangjing Biotechnology (Yangzhou) Co., Ltda7433f39-a8d9-4c78-864d-d7ef193a7daf2025-11-16WarningsExact identifier
application number: M005
Mint Blast Foot and Shoe AntifungalUNDECYLENIC ACID 10%SANSAR, LLCf7fcac19-7b72-4b7a-a28e-669a0eebec9c2025-11-15WarningsExact identifier
application number: M005

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.