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 49 of 62 · 1,235 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
MICONAZOLE Nitrate	MICONAZOLE NITRATE	NuCare Pharmaceuticals,Inc.	fd7dd2eb-03a7-ef1f-e053-6294a90a8557	2025-02-04	Warnings	Exact identifier application number: M005
Molecular AF	TOLNAFTATE	Renu Laboratories, LLC	1b47e687-29cf-48ce-8bc3-ac8f44f05baa	2025-02-03	Warnings	Exact identifier application number: M005
Dermatool Fungal Nail Treatment	TOLNAFTATE 1%	Papalo Group LLC	2d2c0e12-123d-75bd-e063-6394a90ae546	2025-01-31	Warnings	Exact identifier application number: M005
Bestmade Natural Products BM63	CEANOTHUS, KALI MUR, KALI ARS, OOPHRINUM, SELENIUM, THALLIUM, WEISBADEN	Bestmade Natural Products	2cea4552-3700-3da3-e063-6294a90a14b5	2025-01-30	Warnings	Exact identifier unii: 059QF0KO0R
70% Isopropyl Alcohol	ISOPROPYL ALCOHOL	IDO PHARM	d5833c6f-81dd-6ff6-e053-2995a90ac76d	2025-01-30	Warnings	Exact identifier application number: M005
AWAS ALCOHOLSPRAY	ALCOHOL	IDO PHARM	03010837-0289-3e08-e063-6394a90a7d04	2025-01-30	Warnings	Exact identifier application number: M005
ELON Dual Defense Anti Fungal Formula	UNDECYLENIC ACID	Little Giant Holdings LLC	45c4567d-7876-6459-e054-00144ff88e88	2025-01-28	Warnings	Exact identifier application number: M005
DCH Labs Antifungal Jock	MICONAZOLE NITRATE 2%	Derma Care Research Labs, LLC	fc749882-2e1e-cad3-e053-6294a90a33ca	2025-01-27	Warnings	Exact identifier application number: M005
Antifungal Pen	UNDECYLENIC ACID 25%	XF Agencija Limited	a15d4512-0fc6-424f-9dd3-ab433d9b7a26	2025-01-27	Warnings	Exact identifier application number: M005
Mata Hongos	UNDECYLENIC ACID	Vitamex USA, Corp	21ca7edb-dde3-5846-e063-6394a90a3cc0	2025-01-23	Warnings	Exact identifier application number: M005
Povidone Iodine Scrub	POVIDONE-IODINE	Jianerkang Medical Co., Ltd	53cb4c0d-40b5-4cf3-b122-fd6dd654883f	2025-01-23	Warnings	Exact identifier application number: M005
Medics Choice Soothing Eye Wash	PURIFIED WATER	KC Pharmaceuticals, Inc.	10e49808-161e-f4ec-e063-6294a90a1775	2025-01-19	Warnings	Exact identifier unii: 059QF0KO0R
CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE	CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE	Direct Rx	bbf26437-c9b4-d8e6-e053-2a95a90a0062	2025-01-17	Warnings, Adverse reactions	Exact identifier unii: G07GZ97H65
NATUREPLEX TOLNAFTATE ANTIFUNGAL	TOLNAFTATE	Natureplex, LLC	575b8645-9166-4242-a74f-f4aa4acaaf3d	2025-01-15	Warnings	Exact identifier application number: M005
Tobcharm Antifungal Treatment Cream	ANTIFUNGAL TREATMENT CREAM	Guangzhou Zanming Trading Co., Ltd.	2ba241cc-2767-1190-e063-6294a90ac66b	2025-01-13	Warnings	Exact identifier application number: M005
MICONAZOLE Nitrate 2%	MICONAZOLE NITRATE	Akron Pharma Inc.	8933f939-098a-4257-8d9c-4d5c3240e9a6	2025-01-10	Warnings	Exact identifier application number: M005
STERILE WATER	STERILE WATER	HF Acquisition Co. LLC, DBA HealthFirst	74ed2a6f-824c-a1ff-e053-2a91aa0a57c0	2025-01-09	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
STERILE WATER	STERILE WATER	HF Acquisition Co LLC, DBA HealthFirst	77bd3c0f-f4ab-7cfa-e053-2a91aa0a1b83	2025-01-09	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
STERILE WATER	STERILE WATER	HF Acquisition Co LLC, DBA HealthFirst	7610bf80-61b7-982f-e053-2a91aa0ac1bb	2025-01-09	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
ANTI-ITCH FEMININE CARE	HYDROCORTISONE 0.5%	OL PHARMA TECH, LLC Drs PHARMACY	d6fa5ff3-ebdc-222d-e053-2a95a90a88d5	2025-01-09	Warnings	Exact identifier application number: M005

Reported adverse events (FAERS/openFDA)#

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