Home NDC 51672-2001-01 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 Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 51672-2001-1 Miconazole Nitrate 1 in 1 CARTON CREAM 1 5 51672-2001-1 Miconazole Nitrate 15 g in 1 TUBE CREAM 15 5 51672-2001-2 Miconazole Nitrate 1 in 1 CARTON CREAM 1 5 51672-2001-2 Miconazole Nitrate 30 g in 1 TUBE CREAM 30 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51672-2001 MICONAZOLE NITRATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] 4 Current NDC, Legacy NDC, 4 package rows 20241222_7fd4037e-d350-47b7-a7d9-a43b8e366fa0.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Miconazole Nitrate ACTIVE INGREDIENT VW4H1CYW1K MICONAZOLE NITRATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] 2 Miconazole ACTIVE MOIETY 7NNO0D7S5M MICONAZOLE NITRATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] 2 apricot kernel oil INACTIVE INGREDIENT 54JB35T06A MICONAZOLE NITRATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] 2 benzoic acid INACTIVE INGREDIENT 8SKN0B0MIM MICONAZOLE NITRATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] 2 butylated hydroxytoluene INACTIVE INGREDIENT 1P9D0Z171K MICONAZOLE NITRATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] 2 glycol stearate INACTIVE INGREDIENT 0324G66D0E MICONAZOLE NITRATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] 2 mineral oil INACTIVE INGREDIENT T5L8T28FGP MICONAZOLE NITRATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] 2 PEG-32 stearate INACTIVE INGREDIENT 33GX5WQC0M MICONAZOLE NITRATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] 2 PEG-6 stearate INACTIVE INGREDIENT 8LQC57C6B0 MICONAZOLE NITRATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] 2 polyethylene glycol 300 INACTIVE INGREDIENT 5655G9Y8AQ MICONAZOLE NITRATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] 2 water INACTIVE INGREDIENT 059QF0KO0R MICONAZOLE NITRATE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] 2
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 57 of 70 · 1,400 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join PhysiciansCare Ophthalmic Solution Eyewash Purified Water, 98.3% PURIFIED WATER 98.3% Acme United Corporation 9248ee71-2d47-620d-e053-2995a90af5c8 2024-11-26 Warnings Exact identifier unii: 059QF0KO0R PhysiciansCare Ophthalmic Solution Eyewash PURIFIED WATER 98.3% Acme United Corporation cca454e0-b2bd-4215-bc06-426fcc3f7bd6 2024-11-26 Warnings Exact identifier unii: 059QF0KO0R PhysiciansCare Ophthalmic Solution Eyewash PURIFIED WATER 98.3% Acme United Corporation d3812fa3-9334-464d-b50c-98548ff76727 2024-11-26 Warnings Exact identifier unii: 059QF0KO0R DANGTTEOL MINERAL WATER AQBC CO., LTD 27db14a9-3812-433f-e063-6394a90a11e7 2024-11-26 Warnings Exact identifier unii: 059QF0KO0R Povidone-Iodine POVIDONE-IODINE Mazza Healthcare, LLC 31df570a-35ae-41a2-b04a-fce65e9d596d 2024-11-21 Warnings Exact identifier application number: M005 Povidone-Iodine POVIDONE-IODINE Mazza Healthcare, LLC 3dc3303f-54b2-4aec-8568-5e0f8eb7cb14 2024-11-21 Warnings Exact identifier application number: M005 WINCO ANTIFUNGAL TOLNAFTATE 1% WinCo Foods LLC 46b58c71-d62e-4b3d-b2ec-65407032eeea 2024-11-21 Warnings Exact identifier application number: M005 Dynarex Antifungal ANTIFUNGAL Dynarex Corporation ab5b6467-c158-4407-9d52-3c0731030680 2024-11-20 Warnings Exact identifier application number: M005 4718 Enema, Mineral Oil 4718 ENEMA, MINERAL OIL Dynarex 9e51c852-9477-5cf5-e053-2a95a90a97db 2024-11-20 Warnings Exact identifier unii: T5L8T28FGP Terrasil JockItch Treatment Maximum Strength CLOTRIMAZOLE Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions 8afe11c1-0a85-4255-8eba-e8cbde0759a0 2024-11-20 Warnings Exact identifier application number: M005 Terrasil Ringworm Treatment MAX CLOTRIMAZOLE Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions fc2b740a-49c1-4a01-a94c-8cade52a2b82 2024-11-20 Warnings Exact identifier application number: M005 MICONAZOLE NITRATE MICONAZOLE NITRATE ALLIED TRADE LINK LLC 25520dba-0159-2a3f-e063-6294a90a4c33 2024-11-12 Warnings Exact identifier application number: M005 unii: VW4H1CYW1K MONISTAT 7 7-DAY DISPOSABLE APPLICATORS MICONAZOLE NITRATE Insight Pharmaceuticals LLC c4b68aff-e95f-47ae-b190-6a671bef1877 2024-11-12 Warnings Exact identifier unii: VW4H1CYW1K Crane Safety Eye Wash WATER SOLUTION Crane Safety LLC 96d8dda9-6cd6-3f68-e053-2995a90a0da2 2024-11-08 Warnings Exact identifier unii: 059QF0KO0R CLOTRIMAZOLE CLOTRIMAZOLE ALLIED TRADE LINK LLC 266d7b94-2954-4831-e063-6394a90a3f33 2024-11-08 Warnings Exact identifier application number: M005 RUGBY EYE WASH WATER, PURIFIED A-S Medication Solutions 0773e558-2f46-494c-888a-3bc517202b65 2024-11-08 Warnings Exact identifier unii: 059QF0KO0R Antifungal TOLNAFTATE 1% Chain Drug Marketing Association Inc. 26303499-dc58-f417-e063-6394a90a0a1b 2024-11-05 Warnings Exact identifier application number: M005 Miconazole 7 MICONAZOLE NITRATE P & L Development, LLC facc7b65-0376-445a-8a3d-5180f2f9d5ff 2024-11-05 Warnings Exact identifier unii: VW4H1CYW1K AZOLEN MICONAZOLE NITRATE STRATUS PHARMACEUTICALS INC 3264bd0a-c628-404b-8c09-8586682d054e 2024-10-31 Warnings Exact identifier application number: M005 unii: VW4H1CYW1K BACITRACIN ZINC BACITRACIN ZINC STRATUS PHARMACEUTICALS INC b2cb3a96-b0ca-42ee-8056-91d5450fb376 2024-10-31 Warnings Exact identifier application number: M005
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.