Athletes Foot

Product NDC: 70084-510
11-digit product format: 700840510
Labeler code: 70084
Product ID: 70084-510_419d881a-db12-b5bd-e063-6294a90a0ea4
Type: HUMAN OTC DRUG
Nonproprietary name: Tolnaftate
Dosage form: CREAM
Route: TOPICAL
Labeler: Quantum, Inc.
Application: M005
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2005-12-05
Substance: TOLNAFTATE
Active strength: 10 mg/g
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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 · 24 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	70084-510-01	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	70084-510-01	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	70084-510-01	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	70084-510-01	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	70084-510-01	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	70084-510-01	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	70084-510-01	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	70084-510-01	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	70084-510-01	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	70084-510-01	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	70084-510-01	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded product	product		I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	70084-510-01	I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`

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: Athletes Foot
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
TOLNAFTATE	10 mg/g

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
103951	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
6cb95707-9831-41f1-a23e-9e3356141fdc	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2025-01-30	Athlete's Foot
2025-01-30	Athlete's Foot
2023-02-13	Athlete's Foot
2023-02-13	Athlete's Foot
2021-01-29	Athlete's Foot
2021-01-29	Athlete's Foot

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70084-510-01	Athletes Foot	21 g in 1 TUBE	CREAM	21		4
70084-510-01	Athletes Foot	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
70084-510	ATHLETES FOOT (TOLNAFTATE) CREAM [QUANTUM, INC.]	3	Current NDC, Legacy NDC, 2 package rows	20230214_6cb95707-9831-41f1-a23e-9e3356141fdc.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 18 of 49 · 973 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Triple Antifungal	MICONAZOLE NITRATE	Advantice Health, LLC	9a47fb1b-a41f-4c8a-8e43-7332853c308e	2026-03-19	Warnings	Exact identifier application number: M005
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

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
103951	tolnaftate 1 % Topical Cream	PSN	6cb95707-9831-41f1-a23e-9e3356141fdc	4
103951	tolnaftate 10 MG/ML Topical Cream	SCD	6cb95707-9831-41f1-a23e-9e3356141fdc	4
103951	tolnaftate 1 % Topical Cream	SY	6cb95707-9831-41f1-a23e-9e3356141fdc	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
70084-510-01	70084051001	1 TUBE in 1 CARTON (70084-510-01) / 21 g in 1 TUBE	1 tube	2005-12-05	No	No	Current