Clotrimazole

Product NDC: 51672-2002
11-digit product format: 516722002
Labeler code: 51672
Product ID: 51672-2002_390cee55-c38f-accf-e063-6294a90ab7f7
Type: HUMAN OTC DRUG
Nonproprietary name: Clotrimazole
Dosage form: CREAM
Route: TOPICAL
Labeler: Sun Pharmaceutical Industries, Inc.
Application: M005
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 1995-06-01
Substance: CLOTRIMAZOLE
Active strength: 1 g/100g
Pharmacologic classes: Azole Antifungal [EPC], Azoles [CS]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: Clotrimazole
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
CLOTRIMAZOLE	1 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
G07GZ97H65	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
309367	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
a3a5cbf5-cabb-48d8-8877-74a97f7c0f57	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
b64d2752-34ef-378a-1f4f-8bff32b0d1ae	Product name	4	20250626
cb7783e0-feaa-7e56-fb3b-d43b6efa77c9	Product name	2	20250121
3c386306-c48a-413e-bb69-70cb268496f3	Product name	1	20210727
f31c883b-7ebf-1c60-f3b6-4ba41e8ff7a6	Product name	2	20151106
9869efd7-d6dd-0665-5b67-53adbe6ef15e	Product name	1	20140508
f5395dd2-4395-d8c6-3477-8c2d4a2f951c	Product name	1	20140508

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 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

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

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 44 of 49 · 973 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Dr. Rainer s Vaginal Cream	MICONAZOLE NITRATE	Plexoris Health Care Products, Llc	1f0ee635-c70d-4194-a01d-370ca5c22fcd	2024-12-11	Warnings	Exact identifier application number: M005
BOA VIDA Antifungal	MICONAZOLE NITRATE	Central Solutions Inc	69c5340d-9abd-43bf-a90b-9568d615f06f	2024-12-09	Warnings	Exact identifier application number: M005
BLUESEA DISPOSABLE HAND SANITIZER	ALCOHOL	BLUE SEA AEROSOL & DAILY CARE CO., LTD	7a552be2-a9e1-4c6f-b1c2-79113a73bd2f	2024-12-06	Warnings	Exact identifier application number: M005
U HAND SANITIZER CLASSIC	BENZALKONIUM CHLORIDE	BLUE SEA AEROSOL & DAILY CARE CO., LTD	fbc27a24-0e81-4907-b24f-881c4fe0ec44	2024-12-06	Warnings	Exact identifier application number: M005
BLUESEA INSTANT HAND SANITIZER	ALCOHOL	BLUE SEA AEROSOL & DAILY CARE CO., LTD	e6b5ce49-d6d6-4b24-8b40-bfb1fb7005bd	2024-12-06	Warnings	Exact identifier application number: M005
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
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
CLOTRIMAZOLE	CLOTRIMAZOLE	ALLIED TRADE LINK LLC	266d7b94-2954-4831-e063-6394a90a3f33	2024-11-08	Warnings	Exact identifier application number: M005
Antifungal	TOLNAFTATE 1%	Chain Drug Marketing Association Inc.	26303499-dc58-f417-e063-6394a90a0a1b	2024-11-05	Warnings	Exact identifier application number: M005
AZOLEN	MICONAZOLE NITRATE	STRATUS PHARMACEUTICALS INC	3264bd0a-c628-404b-8c09-8586682d054e	2024-10-31	Warnings	Exact identifier application number: M005
BACITRACIN ZINC	BACITRACIN ZINC	STRATUS PHARMACEUTICALS INC	b2cb3a96-b0ca-42ee-8056-91d5450fb376	2024-10-31	Warnings	Exact identifier application number: M005
Premier Value Antifungal Maximum Strength	UNDECYLENIC ACID	PHARMACY VALUE ALLIANCE, LLC	f5694ee5-616c-40f6-8da4-c3620dbcd6f7	2024-10-28	Warnings	Exact identifier application number: M005
Clotrimazole 1%	CLOTRIMAZOLE	Chain Drug Marketing Association Inc.	24ff5ad7-2ff9-b254-e063-6394a90a27a7	2024-10-21	Warnings	Exact identifier application number: M005
Micomitin Antifungal	TOLNAFTATE	PureTek Corporation	de9842ba-0254-8ae1-e053-2995a90a0664	2024-10-16	Warnings	Exact identifier application number: M005
Ongo - Fin	TOLNAFTATE	Efficient Laboratories Inc.	bb5fb71f-bee0-42fa-9c9f-6231b555324c	2024-10-14	Warnings	Exact identifier application number: M005

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
G07GZ97H65	CLOTRIMAZOLE	23593-75-1	CLOTRIMAZOLE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
309367	clotrimazole 1 % Topical Cream	PSN	1e7e74f6-9bca-48ab-804a-a7a81df3b608	7
309367	clotrimazole 1 % Topical Cream	PSN	9afb964c-9b88-4701-adcf-7070e25cb6c1	7
309367	clotrimazole 10 MG/ML Topical Cream	SCD	1e7e74f6-9bca-48ab-804a-a7a81df3b608	7
309367	clotrimazole 10 MG/ML Topical Cream	SCD	9afb964c-9b88-4701-adcf-7070e25cb6c1	7
309367	clotrimazole 1 % Topical Cream	SY	1e7e74f6-9bca-48ab-804a-a7a81df3b608	7
309367	clotrimazole 1 % Topical Cream	SY	9afb964c-9b88-4701-adcf-7070e25cb6c1	7
309367	clotrimazole 1 % Topical Cream	PSN	ba1dc4a4-073f-4f30-bb9c-9ed043700431	6
309367	clotrimazole 10 MG/ML Topical Cream	SCD	ba1dc4a4-073f-4f30-bb9c-9ed043700431	6
309367	clotrimazole 1 % Topical Cream	SY	ba1dc4a4-073f-4f30-bb9c-9ed043700431	6
309367	clotrimazole 1 % Topical Cream	PSN	70e1efac-1738-43db-b19c-bbe02810b6e7	5
309367	clotrimazole 10 MG/ML Topical Cream	SCD	70e1efac-1738-43db-b19c-bbe02810b6e7	5
309367	clotrimazole 1 % Topical Cream	SY	70e1efac-1738-43db-b19c-bbe02810b6e7	5
309367	clotrimazole 1 % Topical Cream	PSN	a3a5cbf5-cabb-48d8-8877-74a97f7c0f57	4
309367	clotrimazole 10 MG/ML Topical Cream	SCD	a3a5cbf5-cabb-48d8-8877-74a97f7c0f57	4
309367	clotrimazole 1 % Topical Cream	SY	a3a5cbf5-cabb-48d8-8877-74a97f7c0f57	4
309367	clotrimazole 1 % Topical Cream	PSN	b69db78b-5f10-8ca2-e053-2a95a90ac88c	2
309367	clotrimazole 1 % Topical Cream	PSN	01b1b76f-0c11-437f-82b5-931670c27a8d	2
309367	clotrimazole 10 MG/ML Topical Cream	SCD	b69db78b-5f10-8ca2-e053-2a95a90ac88c	2
309367	clotrimazole 10 MG/ML Topical Cream	SCD	01b1b76f-0c11-437f-82b5-931670c27a8d	2
309367	clotrimazole 1 % Topical Cream	SY	b69db78b-5f10-8ca2-e053-2a95a90ac88c	2
309367	clotrimazole 1 % Topical Cream	SY	01b1b76f-0c11-437f-82b5-931670c27a8d	2
309367	clotrimazole 1 % Topical Cream	PSN	8fcf70e8-70e2-4b41-99c0-a351b2c3a2a0	1
309367	clotrimazole 1 % Topical Cream	PSN	8e1058cf-1bd4-4c81-81a5-3a1754caca3f	1
309367	clotrimazole 1 % Topical Cream	PSN	deaa88bc-f7b0-16e2-e053-2995a90ac45a	1
309367	clotrimazole 10 MG/ML Topical Cream	SCD	8fcf70e8-70e2-4b41-99c0-a351b2c3a2a0	1
309367	clotrimazole 10 MG/ML Topical Cream	SCD	8e1058cf-1bd4-4c81-81a5-3a1754caca3f	1
309367	clotrimazole 10 MG/ML Topical Cream	SCD	deaa88bc-f7b0-16e2-e053-2995a90ac45a	1
309367	clotrimazole 1 % Topical Cream	SY	8fcf70e8-70e2-4b41-99c0-a351b2c3a2a0	1
309367	clotrimazole 1 % Topical Cream	SY	8e1058cf-1bd4-4c81-81a5-3a1754caca3f	1
309367	clotrimazole 1 % Topical Cream	SY	deaa88bc-f7b0-16e2-e053-2995a90ac45a	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
51672-2002-1	51672200201	1 TUBE in 1 CARTON (51672-2002-1) / 15 g in 1 TUBE	1 tube	1995-06-01	0000-00-00	No	No	Current
51672-2002-2	51672200202	1 TUBE in 1 CARTON (51672-2002-2) / 30 g in 1 TUBE	1 tube	1995-06-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Clotrimazole Cream USP,1% Antifungal Cream	Preferred Pharmaceuticals Inc.	2026-04-01	HUMAN OTC DRUG LABEL	5
Clotrimazole Cream USP,1% Antifungal Cream	A-S Medication Solutions	2025-12-05	HUMAN OTC DRUG LABEL	7
Clotrimazole Cream USP,1% Antifungal Cream	A-S Medication Solutions	2025-11-19	HUMAN OTC DRUG LABEL	7
Clotrimazole Cream USP,1% Antifungal Cream	Sun Pharmaceutical Industries, Inc. \| Sun Pharma Canada Inc.	2025-07-03	HUMAN OTC DRUG LABEL	4
Clotrimazole Cream USP,1% Antifungal Cream	A-S Medication Solutions	2025-01-22	HUMAN OTC DRUG LABEL	3
Clotrimazole Cream USP,1% Antifungal Cream	Proficient Rx LP	2024-01-01	HUMAN OTC DRUG LABEL	6
Clotrimazole Cream USP,1% Antifungal Cream	NuCare Pharmaceuticals,Inc.	2022-05-10	HUMAN OTC DRUG LABEL	1
Clotrimazole Cream USP,1% Antifungal Cream	REMEDYREPACK INC.	2022-03-25	HUMAN OTC DRUG LABEL	1
Clotrimazole Cream USP,1% Antifungal Cream	NuCare Pharmaceuticals,Inc.	2022-01-14	HUMAN OTC DRUG LABEL	2
Clotrimazole Cream USP,1% Antifungal Cream	Central Texas Community Health Centers \| Travis County Healthcare District	2018-06-07	HUMAN OTC DRUG LABEL	2
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	1
Clotrimazole Cream USP,1% Antifungal Cream	Rebel Distributors Corp	2011-02-09	HUMAN OTC DRUG LABEL	1