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		2026-10-21

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 18 of 49 · 969 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Antifungal	CLOTRIMAZOLE	Dynarex Corporation	4d4cc4b4-c0b4-9e25-e063-6294a90a70b8	2026-03-18	Warnings	Exact identifier application number: M005
Antifungal	MICONAZOLE NITRATE	Dynarex Corporation	4d384385-f3c5-09ba-e063-6394a90aec7f	2026-03-17	Warnings	Exact identifier application number: M005
Fungi Nail Toe and Foot	TOLNAFTATE	Kramer Laboratories	e21ccb83-54ff-4605-80bf-7b4b789c7cb7	2026-03-17	Warnings	Exact identifier application number: M005
Peunitory Fungal Nail Treatment	TOLNAFTATE 1%	Guangzhou Huixue Biotechnology Co., Ltd.	4d2e86bc-5122-ba4a-e063-6394a90acf13	2026-03-16	Warnings	Exact identifier application number: M005
DRMITSUI FOOT ANTIFUNGAL TREATMENT	SALICYLIC ACID	Zhenping Renren Industry Co., Ltd.	4ce59d31-56fe-d74f-e063-6294a90a7cce	2026-03-14	Warnings	Exact identifier application number: M005
NERANTE FUNGUS NAIL PEN	UNDECYLENIC ACID	Guangdong Quadrant Ecological Technology Co., Ltd.	4ce3984b-53cd-a665-e063-6394a90afe5f	2026-03-13	Warnings	Exact identifier application number: M005
FUNGAL NAIL TREATMENT	UNDECYLENIC ACID	Guangdong Quadrant Ecological Technology Co., Ltd.	4ce3f0e2-b532-b89f-e063-6294a90a7e25	2026-03-13	Warnings	Exact identifier application number: M005
BYT BANGYTONG HELPS WITH NAGELPILZ	TOLNAFTATE 1% HELPS WITH NAGELPILZ LIQUID	Shenzhen Jindali Technology Co., Ltd	49ed1cc8-e8e5-399c-e063-6394a90a044a	2026-03-10	Warnings	Exact identifier application number: M005
Natouch Antifungal Wipes Plus	ANTIFUNGAL ANTISEPTIC WIPES PLUS	Natouch LLC	a85cb307-b3ad-1584-e053-2995a90a9a70	2026-03-10	Warnings	Exact identifier application number: M005
Tuymec Antifungal Medicated Bar	ANTIFUNGAL MEDICATED BAR	Guangzhou Jingliang Cosmetics Co., Ltd.	4cb6fdfd-116e-14e9-e063-6294a90a4de3	2026-03-10	Warnings	Exact identifier application number: M005
Tuymec Antifungal Medicated Bar	ANTIFUNGAL MEDICATED BAR	Guangzhou Jingliang Cosmetics Co., Ltd.	4cb73ebe-f9bb-5a8d-e063-6294a90a3c2b	2026-03-10	Warnings	Exact identifier application number: M005
SootheSense Toenail Fungus Treatment	UNDECYLENIC ACID	Guangdong Quadrant Ecological Technology Co., Ltd.	4ca2bbeb-3b8a-9482-e063-6294a90a5789	2026-03-09	Warnings	Exact identifier application number: M005
Natouch Antifungal Antiseptic Wipes	ANTIFUNGAL ANTISEPTIC WIPES	Natouch LLC	4c84c556-8d0b-ec28-e063-6294a90af1d3	2026-03-08	Warnings	Exact identifier application number: M005
ANTIFUNGAL Cream	ANGELICA DAHURICA EXTRACTT, ASIATIC ACID	Guangzhou Mizi Biotechnology Co., LTD.	4c586cd9-d356-34d8-e063-6294a90a4d11	2026-03-06	Warnings	Exact identifier application number: M005
FungiFoam	TOLNAFTATE	The Tetra Corporation	2449e8e5-9d7e-4119-9e7a-378efe55f875	2026-03-06	Warnings	Exact identifier application number: M005
RoyceDerm ANTIFUNGAL .soap.	CLOTRIMAZOLE 1%	RoyceDerm LLC	4c43e62b-9060-8962-e063-6394a90aff63	2026-03-05	Warnings	Exact identifier application number: M005
Derman Antifungal	TOLNAFTATE	Compania Internacional de Comercio, S.A.P.I. de C.V.	5784a783-1056-4d50-8d87-2df4f8e16b09	2026-03-05	Warnings	Exact identifier application number: M005
Antifungal Powder	TOLNAFTATE	ARMY & AIR FORCE EXCHANGE SERVICE	4c39e121-4919-a482-e063-6294a90a98cd	2026-03-04	Warnings	Exact identifier application number: M005
ViLLsure Antifungal Pen	UNDECYLENIC ACID 25%ANTIFUNGAL PEN	Jiangxi Yudexi Pharmaceutical Co., LTD	4c28cf04-94ad-8db6-e063-6394a90a2eed	2026-03-03	Warnings	Exact identifier application number: M005
ProClearz Maximum Strength Fungal Shield Brush-on Antifungal	TOLNAFTATE	Rooftop Consumer Health, Inc.	4d451e87-c25b-49cf-92b8-747b053930c2	2026-03-02	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