Tolnaftate

Product NDC: 56104-001
11-digit product format: 561040001
Labeler code: 56104
Product ID: 56104-001_42785459-fa13-f7a0-e063-6394a90aaac4
Type: HUMAN OTC DRUG
Nonproprietary name: Antifungal Liquid Spray
Dosage form: AEROSOL, SPRAY
Route: TOPICAL
Labeler: Premier Brands of America Inc.
Application: M005
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2013-01-01
Substance: TOLNAFTATE
Active strength: 1.5 g/150g
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	56104-001	56104-001-02	D	Discontinued by firm		2026-10-23

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 23 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	56104-001-02	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	56104-001-02	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	56104-001-02	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	56104-001-53	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	56104-001-02	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	56104-001-53	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	56104-001-02	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	56104-001-53	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	56104-001-02	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	56104-001-53	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	56104-001-02	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	56104-001-53	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	56104-001-02	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	56104-001-53	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	56104-001-02	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	56104-001-53	`0efc9e666f02…`	`f202fb6c5f17…`

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: Tolnaftate
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
TOLNAFTATE	1.5 g/150g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
06KB629TKV	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
313421	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
7a6a63cd-e87d-4229-8acf-b65d63909eb6	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
56104-001-02	Tolnaftate	150 g in 1 CANISTER	AEROSOL, SPRAY	150		11
56104-001-53	Tolnaftate	150 g in 1 CANISTER	AEROSOL, SPRAY	150		11

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
TOLNAFTATE	ACTIVE INGREDIENT	06KB629TKV	TOLNAFTATE (ANTIFUNGAL LIQUID SPRAY) AEROSOL, SPRAY [PREMIER BRANDS OF AMERICA INC.]	1
TOLNAFTATE	ACTIVE MOIETY	06KB629TKV	TOLNAFTATE (ANTIFUNGAL LIQUID SPRAY) AEROSOL, SPRAY [PREMIER BRANDS OF AMERICA INC.]	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	TOLNAFTATE (ANTIFUNGAL LIQUID SPRAY) AEROSOL, SPRAY [PREMIER BRANDS OF AMERICA INC.]	1
BUTYLATED HYDROXYTOLUENE	INACTIVE INGREDIENT	1P9D0Z171K	TOLNAFTATE (ANTIFUNGAL LIQUID SPRAY) AEROSOL, SPRAY [PREMIER BRANDS OF AMERICA INC.]	1
ISOBUTANE	INACTIVE INGREDIENT	BXR49TP611	TOLNAFTATE (ANTIFUNGAL LIQUID SPRAY) AEROSOL, SPRAY [PREMIER BRANDS OF AMERICA INC.]	1
PPG-12-BUTETH-16	INACTIVE INGREDIENT	58CG7042J1	TOLNAFTATE (ANTIFUNGAL LIQUID SPRAY) AEROSOL, SPRAY [PREMIER BRANDS OF AMERICA INC.]	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 35 of 49 · 969 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
SUNMARK MICONAZOLE NITRATE antifungal	MICONAZOLE NITRATE	Strategic Sourcing Services LLC	7c15d95a-5b89-4789-8c91-3f61d7ec7707	2025-07-30	Warnings	Exact identifier application number: M005
Antifungal	MICONAZOLE NITRATE	Advanced Rx LLC	e13eb653-3916-444a-ae86-1738c0308b79	2025-07-28	Warnings	Exact identifier application number: M005
Meridian Unwrapped Antibacterial Deodorant	BENZETHONIUM CHLORIDE	Yangzhou Hongshengding Chemical Co.,Ltd.	a2b9570f-312c-4f46-994d-efe057b247aa	2025-07-28	Warnings	Exact identifier application number: M005
Meridian Antibacterial Deodorant	BENZETHONIUM CHLORIDE	Yangzhou Hongshengding Chemical Co.,Ltd.	b41b130f-48fd-47d4-a94e-74433ae44de2	2025-07-28	Warnings	Exact identifier application number: M005
Rugby Clotrimazole Antifungal Cream	CLOTRIMAZOLE	Preferred Pharmaceuticals Inc.	bd567e91-7152-4612-83e0-8e8a00c2d2c5	2025-07-25	Warnings	Exact identifier application number: M005
Hongocura	UNDECYLENIC ACID, ZINC UNDECYLENATE	MENPER DISTRIBUTORS, INC.	c69b735e-0ffe-4328-bd9f-3c1ac6798c08	2025-07-22	Warnings	Exact identifier application number: M005
Hongocura Pinceladas	UNDECYLENIC ACID	Menper Distributors, Inc.	4b9a3a70-d646-47c6-b969-5c4d759d23a4	2025-07-22	Warnings	Exact identifier application number: M005
Hongocura M	UNDECYLENIC ACID	MENPER DISTRIBUTORS, INC.	b4adb7b0-59b4-4b3c-9b0e-1869bb543174	2025-07-22	Warnings	Exact identifier application number: M005
Hongocura S	UNDECYLENIC ACID	MENPER DISTRIBUTORS, INC.	4a21f371-bfc1-4e66-af16-55b3283872b7	2025-07-22	Warnings	Exact identifier application number: M005
FifthPulse Miconazole Nitrate Cream 1oz	MICONAZOLE NITRATE	Front Pharmaceutical PLC	3a37a3a8-9d05-926c-e063-6294a90a9ed8	2025-07-18	Warnings	Exact identifier application number: M005
FifthPulse Miconazole Nitrate Cream 4oz	MICONAZOLE NITRATE	Front Pharmaceutical PLC	3a382b79-dde9-dde0-e063-6294a90a53bb	2025-07-18	Warnings	Exact identifier application number: M005
FifthPulse clotrimazole cream 4oz	CLOTRIMAZOLE 1%	Front Pharmaceutical PLC	3a389093-48f2-29cb-e063-6294a90ada37	2025-07-18	Warnings	Exact identifier application number: M005
PHARMBANNER Tea Tree Oil Antifungal Soap.	TEA TREE OIL ANTIFUNGAL SOAP.	Shenzhen Xinxin Yunhai Technology Co., Ltd.	3a0860b0-346e-7024-e063-6394a90ace81	2025-07-16	Warnings	Exact identifier application number: M005
TopCare Antifungal	CLOTRIMAZOLE	Topco Associates LLC	6757eb2a-73e0-4bd0-a332-5713fdf3445d	2025-07-16	Warnings	Exact identifier application number: M005
UpandUp Clotrimazole	CLOTRIMAZOLE	Target Corporation	cb2b7d38-9988-493b-9843-56c2f59eed2f	2025-07-16	Warnings	Exact identifier application number: M005
Jock Itch	CLOTRIMAZOLE	TARGET Corporation	1ae551e7-69de-4eef-b4f7-5e1a880e631d	2025-07-16	Warnings	Exact identifier application number: M005
Athletes Foot	CLOTRIMAZOLE	FRED'S, INC.	d2d8f44e-2dfa-446b-855e-86e0d6d2d0df	2025-07-15	Warnings	Exact identifier application number: M005
Tolnaftate Antifungal	TOLNAFTATE	STRATEGIC SOURCING SERVICES LLC	97ffb6fd-5670-4783-b805-88fe9e43ca96	2025-07-15	Warnings	Exact identifier application number: M005
Miconazole Nitrate	MICONAZOLE NITRATE	STRATEGIC SOURCING SERVICES LLC	966a1000-3b08-4f2c-a9f8-568f2524b717	2025-07-15	Warnings	Exact identifier application number: M005
Tolnaftate Antifungal	TOLNAFTATE	Amerisource Bergen	a3c9b783-4a36-46b3-a0dc-0696907eaebb	2025-07-15	Warnings	Exact identifier application number: M005

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
06KB629TKV	TOLNAFTATE	2398-96-1	TOLNAFTATE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
313421	tolnaftate 1 % Topical Spray	PSN	7a6a63cd-e87d-4229-8acf-b65d63909eb6	11
313421	tolnaftate 10 MG/ML Topical Spray	SCD	7a6a63cd-e87d-4229-8acf-b65d63909eb6	11
313421	tolnaftate 1 % Topical Spray	SY	7a6a63cd-e87d-4229-8acf-b65d63909eb6	11

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
56104-001-02	56104000102	150 g in 1 CANISTER (56104-001-02)	150 g	2013-01-01	0000-00-00	No	No	Current
56104-001-53	56104000153	150 g in 1 CANISTER (56104-001-53)	150 g	2013-01-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Premier Brands Tolnaftate Liquid Spray	Premier Brands of America Inc.	2025-10-31	HUMAN OTC DRUG LABEL	11