NDC 51672-2002-01 - Clotrimazole

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: 51672-2002
Requested NDC: 51672-2002-01
Package NDCs from labels: 51672-2002-1, 51672-2002-2, 51672-2002-01
Manufacturer: Preferred Pharmaceuticals Inc.
Effective date: 2026-04-01
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Clotrimazole Cream USP,1% Antifungal Cream	Preferred Pharmaceuticals Inc.	2026-04-01	HUMAN OTC DRUG LABEL
Clotrimazole - A-S Medication Solutions	A-S Medication Solutions	2025-12-05	HUMAN OTC DRUG LABEL
Clotrimazole - A-S Medication Solutions	A-S Medication Solutions	2025-11-19	HUMAN OTC DRUG LABEL
Clotrimazole Cream USP,1% Antifungal Cream	Sun Pharmaceutical Industries, Inc. \| Sun Pharma Canada Inc.	2025-07-03	HUMAN OTC DRUG LABEL
Clotrimazole - A-S Medication Solutions	A-S Medication Solutions	2025-01-22	HUMAN OTC DRUG LABEL
Clotrimazole - Proficient Rx LP	Proficient Rx LP	2024-01-01	HUMAN OTC DRUG LABEL
Clotrimazole Cream USP,1% Antifungal Cream	NuCare Pharmaceuticals,Inc.	2022-05-10	HUMAN OTC DRUG LABEL
Clotrimazole Cream USP,1% Antifungal Cream	REMEDYREPACK INC.	2022-03-25	HUMAN OTC DRUG LABEL
Clotrimazole Cream USP,1% Antifungal Cream	NuCare Pharmaceuticals,Inc.	2022-01-14	HUMAN OTC DRUG LABEL
Clotrimazole Cream USP,1% Antifungal Cream	Central Texas Community Health Centers \| Travis County Healthcare District	2018-06-07	HUMAN OTC DRUG LABEL
Clotrimazole Cream USP,1% Antifungal Cream	H.J. Harkins Company, Inc. \| Taro Pharmaceuticals U.S.A., Inc. \| Taro Pharmaceuticals Inc.	2011-10-14	HUMAN OTC DRUG LABEL
Clotrimazole - Rebel Distributors Corp	Rebel Distributors Corp	2011-02-09	HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
51672-2002-1	Clotrimazole	15 g in 1 TUBE	CREAM	15	4
51672-2002-1	Clotrimazole	1 in 1 CARTON	CREAM	1	4
51672-2002-2	Clotrimazole	30 g in 1 TUBE	CREAM	30	4
51672-2002-2	Clotrimazole	1 in 1 CARTON	CREAM	1	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51672-2002	CLOTRIMAZOLE CREAM [TARO PHARMACEUTICALS U.S.A., INC.]	3	Current NDC, Legacy NDC, 4 package rows	20241115_a3a5cbf5-cabb-48d8-8877-74a97f7c0f57.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
51672-2002-1	GM - Gram	51672-2002	4c2e5eee-4d44-4728-9055-74c57d453259	1	2012-07-24
51672-2002-2	GM - Gram	51672-2002	88f9179a-bac8-4b62-817d-35adddf30d70	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Clotrimazole	ACTIVE INGREDIENT	G07GZ97H65	CLOTRIMAZOLE CREAM [PROFICIENT RX LP]	1
Clotrimazole	ACTIVE INGREDIENT	G07GZ97H65	CLOTRIMAZOLE CREAM [TARO PHARMACEUTICALS U.S.A., INC.]	1
Clotrimazole	ACTIVE INGREDIENT	G07GZ97H65	CLOTRIMAZOLE CREAM [H.J. HARKINS COMPANY, INC.]	1
Clotrimazole	ACTIVE INGREDIENT	G07GZ97H65	CLOTRIMAZOLE CREAM [REBEL DISTRIBUTORS CORP]	1
Clotrimazole	ACTIVE MOIETY	G07GZ97H65	CLOTRIMAZOLE CREAM [REBEL DISTRIBUTORS CORP]	1
Clotrimazole	ACTIVE MOIETY	G07GZ97H65	CLOTRIMAZOLE CREAM [TARO PHARMACEUTICALS U.S.A., INC.]	1
Clotrimazole	ACTIVE MOIETY	G07GZ97H65	CLOTRIMAZOLE CREAM [PROFICIENT RX LP]	1
Clotrimazole	ACTIVE MOIETY	G07GZ97H65	CLOTRIMAZOLE CREAM [H.J. HARKINS COMPANY, INC.]	1
benzyl alcohol	INACTIVE INGREDIENT	LKG8494WBH	CLOTRIMAZOLE CREAM [REBEL DISTRIBUTORS CORP]	1
benzyl alcohol	INACTIVE INGREDIENT	LKG8494WBH	CLOTRIMAZOLE CREAM [PROFICIENT RX LP]	1
benzyl alcohol	INACTIVE INGREDIENT	LKG8494WBH	CLOTRIMAZOLE CREAM [TARO PHARMACEUTICALS U.S.A., INC.]	1
benzyl alcohol	INACTIVE INGREDIENT	LKG8494WBH	CLOTRIMAZOLE CREAM [H.J. HARKINS COMPANY, INC.]	1
cetostearyl alcohol	INACTIVE INGREDIENT	2DMT128M1S	CLOTRIMAZOLE CREAM [PROFICIENT RX LP]	1
cetostearyl alcohol	INACTIVE INGREDIENT	2DMT128M1S	CLOTRIMAZOLE CREAM [TARO PHARMACEUTICALS U.S.A., INC.]	1
cetostearyl alcohol	INACTIVE INGREDIENT	2DMT128M1S	CLOTRIMAZOLE CREAM [H.J. HARKINS COMPANY, INC.]	1
cetostearyl alcohol	INACTIVE INGREDIENT	2DMT128M1S	CLOTRIMAZOLE CREAM [REBEL DISTRIBUTORS CORP]	1
cetyl esters wax	INACTIVE INGREDIENT	D072FFP9GU	CLOTRIMAZOLE CREAM [TARO PHARMACEUTICALS U.S.A., INC.]	1
cetyl esters wax	INACTIVE INGREDIENT	D072FFP9GU	CLOTRIMAZOLE CREAM [PROFICIENT RX LP]	1
cetyl esters wax	INACTIVE INGREDIENT	D072FFP9GU	CLOTRIMAZOLE CREAM [H.J. HARKINS COMPANY, INC.]	1
cetyl esters wax	INACTIVE INGREDIENT	D072FFP9GU	CLOTRIMAZOLE CREAM [REBEL DISTRIBUTORS CORP]	1
polysorbate 60	INACTIVE INGREDIENT	CAL22UVI4M	CLOTRIMAZOLE CREAM [PROFICIENT RX LP]	1
polysorbate 60	INACTIVE INGREDIENT	CAL22UVI4M	CLOTRIMAZOLE CREAM [TARO PHARMACEUTICALS U.S.A., INC.]	1
polysorbate 60	INACTIVE INGREDIENT	CAL22UVI4M	CLOTRIMAZOLE CREAM [H.J. HARKINS COMPANY, INC.]	1
polysorbate 60	INACTIVE INGREDIENT	CAL22UVI4M	CLOTRIMAZOLE CREAM [REBEL DISTRIBUTORS CORP]	1
sorbitan monostearate	INACTIVE INGREDIENT	NVZ4I0H58X	CLOTRIMAZOLE CREAM [PROFICIENT RX LP]	1
sorbitan monostearate	INACTIVE INGREDIENT	NVZ4I0H58X	CLOTRIMAZOLE CREAM [TARO PHARMACEUTICALS U.S.A., INC.]	1
sorbitan monostearate	INACTIVE INGREDIENT	NVZ4I0H58X	CLOTRIMAZOLE CREAM [H.J. HARKINS COMPANY, INC.]	1
sorbitan monostearate	INACTIVE INGREDIENT	NVZ4I0H58X	CLOTRIMAZOLE CREAM [REBEL DISTRIBUTORS CORP]	1
water	INACTIVE INGREDIENT	059QF0KO0R	CLOTRIMAZOLE CREAM [TARO PHARMACEUTICALS U.S.A., INC.]	1
water	INACTIVE INGREDIENT	059QF0KO0R	CLOTRIMAZOLE CREAM [H.J. HARKINS COMPANY, INC.]	1
water	INACTIVE INGREDIENT	059QF0KO0R	CLOTRIMAZOLE CREAM [PROFICIENT RX LP]	1
water	INACTIVE INGREDIENT	059QF0KO0R	CLOTRIMAZOLE CREAM [REBEL DISTRIBUTORS CORP]	1

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 33 of 62 · 1,235 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
SKINHEAL ANTIFUNGAL	TOLNAFTATE	Zhejiang Dingtai Pharmaceutical Co., Ltd	570ee9fb-a495-4a99-9215-0cd1bb2e0290	2025-11-10	Warnings	Exact identifier application number: M005
HUA TUO XIAN GAO ANTIFUNGAL	CLOTRIMAZOLE	MADISON ONE ACME INC	e11c4d87-8dc2-44b1-bf6b-12e7ef4f3d1d	2025-11-10	Warnings	Exact identifier application number: M005 unii: G07GZ97H65
Selan Antifungal	SELAN ANTIFUNGAL	Trividia Manufacturing Solutions, Inc	8c7e51a0-0cd5-4ae3-a904-fad7ac6c1a29	2025-11-07	Warnings	Exact identifier application number: M005
Fortinia Ultra	CLOTRIMAZOLE 1%	The Podiatree Company	43065a59-fb81-b1c2-e063-6294a90a36e0	2025-11-07	Warnings	Exact identifier application number: M005 unii: G07GZ97H65
STERILE WATER	WATER	Henry Schein, Inc.	f4087143-9868-4308-b96c-43657ee8ec28	2025-11-07	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
MICOCLEAR	CLOTRIMAZOLE ANTIFUNGAL	Rising Pharma Holdings, Inc.	d75b7d3c-3f1c-47e1-8122-4645f56a444e	2025-11-06	Warnings	Exact identifier application number: M005 rxcui: 309367 unii: G07GZ97H65
Zilactin Early Relief Cold Sore	BENZYL ALCOHOL	ASCENT CONSUMER PRODUCTS, INC	42ef8bfa-c4d9-01cf-e063-6394a90ac88a	2025-11-06	Warnings	Exact identifier unii: LKG8494WBH
Medline	MICONAZOLE NITRATE	Medline Industries, LP	1ea444eb-f2f5-8c63-e063-6294a90acac8	2025-11-06	Warnings	Exact identifier application number: M005
Miconazole Nitrate	ANTIFUNGAL POWDER SPRAY	Premier Brands of America Inc.	38ccf19c-2290-ad99-e063-6394a90a5469	2025-11-06	Warnings	Exact identifier application number: M005
Tolnaftate	ANTIFUNGAL POWDER SPRAY WITH BAKING SODA	Target Corporation	37792b12-c3dc-558f-e063-6294a90a7e75	2025-11-06	Warnings	Exact identifier application number: M005
Tolnafate	TOLNAFTATE POWDER SPRAY	Topco Associates LLC	5f8ae9ab-5e34-7a60-e053-2991aa0a9817	2025-11-06	Warnings	Exact identifier application number: M005
Tolnaftate	TOLNAFTATE JOCK ITCH POWDER SPRAY TALC FREE	Topco Associates LLC	5f8ac6b7-c46c-226c-e053-2991aa0a9606	2025-11-06	Warnings	Exact identifier application number: M005
Tolnaftate	ANTIFUNGAL LIQUID SPRAY	Topco Associates LLC	3dd0df06-3c74-4c34-a69e-4240945f5fa5	2025-11-06	Warnings	Exact identifier application number: M005
Anti-Fungal Powder	MICONAZOLE NITRATE	TopCo Associates	19c3fbc5-abde-57df-e063-6394a90a125c	2025-11-06	Warnings	Exact identifier application number: M005
Tolnaftate	FOOT ODOR CONTROL SPRAY	Topco Associates LLC	17993a9f-0d44-43a1-8608-94ee8a08b539	2025-11-06	Warnings	Exact identifier application number: M005
DVO Estriol cream	ESTRIOL0.2%	Guangzhou Huixue Biotechnology Co., Ltd.	42e4cc84-7c00-6937-e063-6294a90a0c09	2025-11-05	Warnings	Exact identifier application number: M005
Bacteriostatic Water	BACTERIOSTATIC WATER	ProPharma Distribution	42c6938e-f747-ae13-e063-6294a90a59a3	2025-11-04	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
Medline	MICONAZOL NITRATE	Medline Industries, LP	dad58efb-cc20-577a-e053-2a95a90abd9d	2025-11-03	Warnings	Exact identifier application number: M005
Tolnafate	TOLNAFTATE POWDER SPRAY	HEB	c6af941a-0b85-4611-a6f3-b13fcf3c4a87	2025-11-03	Warnings	Exact identifier application number: M005
Tolnaftate	FOOT ODOR CONTROL SPRAY	HEB	c585605b-ecb8-4dd8-9205-a9be02d751fa	2025-11-03	Warnings	Exact identifier application number: M005

Reported adverse events (FAERS/openFDA)#

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