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 46 of 49 · 969 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Secura Protective	ZINC OXIDE	Smith & Nephew Medical Ltd	b077aa64-49a3-42ee-abb3-88f833635b93	2024-06-12	Warnings	Exact identifier application number: M005
clotrimazole	CLOTRIMAZOLE	NuCare Pharmaceuticals,Inc.	627375fb-2f20-16bc-e053-2a91aa0a1542	2024-06-06	Warnings	Exact identifier application number: M005
Clotrimazole	CLOTRIMAZOLE	Cardinal Health 110 dba LEADER	199df107-3384-6e03-e063-6294a90afc38	2024-05-29	Warnings	Exact identifier application number: M005
Femmesil	CLOTRIMAZOLE	Aidance Skincare & Topical Solutions, LLC	efddad82-9dc7-4cd9-b33c-7e85f30d992e	2024-05-24	Warnings	Exact identifier application number: M005
Anti-Fungal	MICONAZOLE NITRATE	Universal Distribution Center LLC	8f316b0d-d308-4ae6-82c4-39bb0d1d474e	2024-05-21	Warnings	Exact identifier application number: M005
CANESPIES	TOLNAFTATE	OPMX LLC	e2f9eedc-3c43-416b-85b5-ba07fb5fb4db	2024-05-17	Warnings	Exact identifier application number: M005
Up and Up Antifungal	TOLNAFTATE 1%	Target Corporation	8f54c8c7-6771-49c3-b429-53aa6df54dc5	2024-05-08	Warnings	Exact identifier application number: M005
Up and Up Athletes Foot	CLOTRIMAZOLE 1%	Target Corporation	52b61859-11ae-4990-aa0c-9dc1dd00adf4	2024-05-08	Warnings	Exact identifier application number: M005
ADI Medical PVP-I Pouch, Foil	POVIDONE-IODINE	Asia Dynamics Inc., d/b/a ADI Medical	0e8baf24-0c67-5511-e063-6394a90acaa1	2024-05-02	Warnings	Exact identifier application number: M005
Caseys Antimicrobial Hand Sanitizer	ETHYL ALCOHOL	Navajo Manufacturing Company Inc.	78863024-390c-4ff9-8ed6-02af07902a30	2024-04-29	Warnings	Exact identifier application number: M005
MQUPIN Liquid Fungal Nail Treatment	LIQUID FUNGAL NAIL TREATMENT	Zhengzhou Miaoqi Medical Technology Co., Ltd.	14782f8c-3b29-1d88-e063-6294a90ac3e4	2024-03-25	Warnings	Exact identifier application number: M005
ETADERM Advanced Antifungal Support	UNDECYLENIC ACID	NUEPHASE LLC	adb12a1c-ece9-4a59-a62c-89d212c57e6f	2024-03-13	Warnings	Exact identifier application number: M005
Dermachange Jock	MICONAZOLE NITRATE	Private label Beauty and Wellness	12eef049-76c9-1450-e063-6394a90a00ea	2024-03-05	Warnings	Exact identifier application number: M005
Clotrimazole Antifungal	CLOTRIMAZOLE	Trifecta Pharmaceuticals USA, LLC.	11bf50db-552e-0a39-e063-6394a90af60d	2024-02-19	Warnings	Exact identifier application number: M005
TOLNAFTATE ANTIFUNGAL	TOLNAFTATE	Bryant Ranch Prepack	fbbd159c-217e-46d3-963c-ba0bd1e9bbe8	2024-01-29	Warnings	Exact identifier application number: M005
Target Jock Itch	CLOTRIMAZOLE 1%	Target Corporation	f44d4c44-99d1-413f-b9c3-8330bdd21abb	2024-01-17	Warnings	Exact identifier application number: M005
FIRST SHIELD	BENZALKONIUM CHLORIDE, LIDOCAINE HCI	Ever Ready First Aid	ee198aa1-ad0d-9185-e053-2a95a90a6595	2024-01-15	Warnings	Exact identifier application number: M005
Ever Ready HAND SANITIZER	ETHYL ALCOHOL	Ever Ready First Aid	ec1af7ef-3c95-9c60-e053-2a95a90acf47	2024-01-15	Warnings	Exact identifier application number: M005
MY MEDIC SUPER SANITIZER	ETHYL ALCOHOL	Sled Distribution, LLC	e7451738-75d5-5dc4-e053-2a95a90a7aee	2024-01-15	Warnings	Exact identifier application number: M005
Medical Super	ALCOHOL	Beijing HKKY Medical Tech. Co., Ltd.	ed2649c6-d971-4338-8745-cd0a40f7b0c2	2024-01-13	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