FungiFoam

Product NDC: 49406-004
11-digit product format: 494060004
Labeler code: 49406
Product ID: 49406-004_4c5c1f4d-1131-c3d0-e063-6394a90a88e2
Type: HUMAN OTC DRUG
Nonproprietary name: TOLNAFTATE
Dosage form: AEROSOL, FOAM
Route: TOPICAL
Labeler: The Tetra Corporation
Application: M005
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2020-07-13
Substance: TOLNAFTATE
Active strength: 10 mg/mL
NDC exclude flag: No
Listing certified through: 2027-12-31
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	49406-004	49406-004-30	D	Discontinued by firm		2026-10-16

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 · 21 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
2025-04-01 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	49406-004-75	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	49406-004-30	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	49406-004-75	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	49406-004-30	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	49406-004-75	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	49406-004-30	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	49406-004-75	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	49406-004-30	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	49406-004-30	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	49406-004-75	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	49406-004-30	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	49406-004-75	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	49406-004-30	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	49406-004-75	U	Excluded because listing certification expired	`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: FungiFoam
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
TOLNAFTATE	10 mg/mL

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 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1356533	Internal RxNorm lookup
1356538	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
2449e8e5-9d7e-4119-9e7a-378efe55f875	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
49406-004-30	2025-08-18	FungiFoam ANTIFUNGAL
49406-004-75	2025-08-18	FungiFoam ANTIFUNGAL
49406-004-30	2025-01-30	FungiFoam ANTIFUNGAL
49406-004-75	2025-01-30	FungiFoam ANTIFUNGAL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
49406-004-30	FungiFoam	30 mL in 1 TUBE	AEROSOL, FOAM	30	19
49406-004-30	FungiFoam	1 in 1 BOX	AEROSOL, FOAM	1	19
49406-004-75	FungiFoam	75 mL in 1 BOTTLE	AEROSOL, FOAM	75	19
49406-004-75	FungiFoam	1 in 1 BOX	AEROSOL, FOAM	1	19

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
49406-004-75	ML - Milliliter	49406-004	3b9c5268-ecd0-43ac-8cb0-0c1e227c1fb6	1	2026-05-22

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
TOLNAFTATE	ACTIVE INGREDIENT	06KB629TKV	FUNGIFOAM (TOLNAFTATE) AEROSOL, FOAM [THE TETRA CORPORATION]	5
TOLNAFTATE	ACTIVE MOIETY	06KB629TKV	FUNGIFOAM (TOLNAFTATE) AEROSOL, FOAM [THE TETRA CORPORATION]	5
ALKYL (C12-15) BENZOATE	INACTIVE INGREDIENT	A9EJ3J61HQ	FUNGIFOAM (TOLNAFTATE) AEROSOL, FOAM [THE TETRA CORPORATION]	5
BUTYLATED HYDROXYTOLUENE	INACTIVE INGREDIENT	1P9D0Z171K	FUNGIFOAM (TOLNAFTATE) AEROSOL, FOAM [THE TETRA CORPORATION]	5
CARBOXYMETHYLCELLULOSE SODIUM	INACTIVE INGREDIENT	K679OBS311	FUNGIFOAM (TOLNAFTATE) AEROSOL, FOAM [THE TETRA CORPORATION]	5
CETEARETH-25	INACTIVE INGREDIENT	8FA93U5T67	FUNGIFOAM (TOLNAFTATE) AEROSOL, FOAM [THE TETRA CORPORATION]	5
CETOSTEARYL ALCOHOL	INACTIVE INGREDIENT	2DMT128M1S	FUNGIFOAM (TOLNAFTATE) AEROSOL, FOAM [THE TETRA CORPORATION]	5
DIETHYLENE GLYCOL MONOETHYL ETHER	INACTIVE INGREDIENT	A1A1I8X02B	FUNGIFOAM (TOLNAFTATE) AEROSOL, FOAM [THE TETRA CORPORATION]	5
ETHYLHEXYLGLYCERIN	INACTIVE INGREDIENT	147D247K3P	FUNGIFOAM (TOLNAFTATE) AEROSOL, FOAM [THE TETRA CORPORATION]	5
JOJOBA OIL	INACTIVE INGREDIENT	724GKU717M	FUNGIFOAM (TOLNAFTATE) AEROSOL, FOAM [THE TETRA CORPORATION]	5
PHENOXYETHANOL	INACTIVE INGREDIENT	HIE492ZZ3T	FUNGIFOAM (TOLNAFTATE) AEROSOL, FOAM [THE TETRA CORPORATION]	5
POLYOXYL 20 CETOSTEARYL ETHER	INACTIVE INGREDIENT	YRC528SWUY	FUNGIFOAM (TOLNAFTATE) AEROSOL, FOAM [THE TETRA CORPORATION]	5
POLYSORBATE 60	INACTIVE INGREDIENT	CAL22UVI4M	FUNGIFOAM (TOLNAFTATE) AEROSOL, FOAM [THE TETRA CORPORATION]	5
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	FUNGIFOAM (TOLNAFTATE) AEROSOL, FOAM [THE TETRA CORPORATION]	5
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	FUNGIFOAM (TOLNAFTATE) AEROSOL, FOAM [THE TETRA CORPORATION]	5
TROLAMINE	INACTIVE INGREDIENT	9O3K93S3TK	FUNGIFOAM (TOLNAFTATE) AEROSOL, FOAM [THE TETRA CORPORATION]	5
UREA	INACTIVE INGREDIENT	8W8T17847W	FUNGIFOAM (TOLNAFTATE) AEROSOL, FOAM [THE TETRA CORPORATION]	5
WATER	INACTIVE INGREDIENT	059QF0KO0R	FUNGIFOAM (TOLNAFTATE) AEROSOL, FOAM [THE TETRA CORPORATION]	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49406-004	FUNGIFOAM (TOLNAFTATE) AEROSOL, FOAM [THE TETRA CORPORATION]	15	Current NDC, Legacy NDC, 4 package rows	20231013_2449e8e5-9d7e-4119-9e7a-378efe55f875.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 45 of 49 · 973 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Hongo Killer	UNDECYLENIC ACID	Efficient Laboratories Inc	5c433182-0c0c-4a0a-8dd8-a14f60e52425	2024-10-14	Warnings	Exact identifier application number: M005
Miconazole nitrate	ANTIFUNGAL MICONAZOLE LIQUID CONTINUOUS SPRAY	Meijer Distribution Inc	6c2ebe17-994d-41c8-bacb-87b6a63b2db4	2024-10-14	Warnings	Exact identifier application number: M005
Miconazole Nitrate	ANTIFUNGAL	McKesson	8dcca44a-16c7-7262-e053-2a95a90a1b23	2024-10-10	Warnings	Exact identifier application number: M005
CAREALL Clotrimazole	CLOTRIMAZOLE	New World Imports, Inc	ebc565bb-e56c-43ba-a5cb-d2fad2aafc4a	2024-10-07	Warnings	Exact identifier application number: M005
Micotrin AL	TOLNAFTATE	PureTek Corporation	cc0fba1e-82c5-42fd-e053-2995a90af249	2024-10-02	Warnings	Exact identifier application number: M005
Mycozyl AL	TOLNAFTATE	PureTek Corporation	b82c9a8a-f6f1-dca6-e053-2995a90a47f9	2024-10-02	Warnings	Exact identifier application number: M005
MY MEDIC SUPER SANITIZER	ALCOHOL	Nantong Health & Beyond Hygienic Products Inc.	f19971b1-2aeb-4c37-82b0-9525026cff7a	2024-10-02	Warnings	Exact identifier application number: M005
Micotrin AC	CLOTRIMAZOLE	PureTek Corporation	cbe4dd18-c9ef-a4e4-e053-2995a90a5289	2024-10-01	Warnings	Exact identifier application number: M005
Micotrin AP	MICONAZOLE NITRATE	PureTek Corporation	cbe3d495-cdee-2343-e053-2a95a90a5b82	2024-10-01	Warnings	Exact identifier application number: M005
Mycozyl AC	CLOTRIMAZOLE	PureTek Corporation	b676d257-3cfd-7f24-e053-2995a90a546e	2024-10-01	Warnings	Exact identifier application number: M005
Mycozyl AP	MICONAZOLE NITRATE	PureTek Corporation	b3c46a30-7ff2-0dc4-e053-2995a90aa571	2024-10-01	Warnings	Exact identifier application number: M005
AOSI HEALTHCARE HAND SANITIZER	ALCOHOL	Nantong Health & Beyond Hygienic Products Inc.	59d631d0-d8ae-45a8-a7a9-26de9cc427b3	2024-09-25	Warnings	Exact identifier application number: M005
Clotrimazole 1%	CLOTRIMAZOLE	Dabur India Limited	22916978-303f-e62a-e063-6394a90a2100	2024-09-20	Warnings	Exact identifier application number: M005
Mentholatum Heel Revival Cream	MENTHOLATUM HEEL REVIVAL CREAM	The Mentholatum Company	21b643c2-eb6e-8939-e063-6394a90aaeac	2024-09-09	Warnings	Exact identifier application number: M005
VAGISTEN-V 7 DAY	MICONAZOLE NITRATE	OPMX LLC	a5bfa501-5ae1-4434-bc31-995d0665b99e	2024-09-04	Warnings	Exact identifier application number: M005
COTTON ON FOUNDATION Tropical Hand Sanitizer	ETHYL ALCOHOL	Nantong Health & Beyond Hygienic Products Inc.	3645359c-06a2-4b97-b982-c54e4a0b8cda	2024-09-04	Warnings	Exact identifier application number: M005
COTTON ON FOUNDATION Coastal Hand Sanitizer	ETHYL ALCOHOL	Nantong Health & Beyond Hygienic Products Inc.	645c09dc-15a4-481f-a605-f12fb8f8e9bd	2024-09-04	Warnings	Exact identifier application number: M005
Publix Athletic Foot	CLOTRIMAZOLE 1%	PUBLIX SUPER MARKETS, INC.	d9f99680-5636-4136-a7c6-c3643339e6b4	2024-08-02	Warnings	Exact identifier application number: M005
ANTIFUNGAL FOOT	TOLNAFTATE	Universal Distribution Center LLC	10579848-5793-4d72-ad5f-62d191c71074	2024-07-16	Warnings	Exact identifier application number: M005
MY MEDIC SUPER SANITIZER	ETHYL ALCOHOL	Nantong Health & Beyond Hygienic Products Inc.	cd8f4ccd-b75e-4de0-87c0-150dfb6e0bf3	2024-07-02	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
1356538	FungiFoam 1 % Topical Foam	PSN	2449e8e5-9d7e-4119-9e7a-378efe55f875	19
1356533	tolnaftate 1 % Topical Foam	PSN	2449e8e5-9d7e-4119-9e7a-378efe55f875	19
1356538	tolnaftate 10 MG/ML Topical Foam [Fungifoam]	SBD	2449e8e5-9d7e-4119-9e7a-378efe55f875	19
1356533	tolnaftate 10 MG/ML Topical Foam	SCD	2449e8e5-9d7e-4119-9e7a-378efe55f875	19
1356538	FungiFoam 1 % Topical Foam	SY	2449e8e5-9d7e-4119-9e7a-378efe55f875	19
1356538	Fungifoam 10 MG/ML Topical Foam	SY	2449e8e5-9d7e-4119-9e7a-378efe55f875	19
1356533	tolnaftate 1 % Topical Foam	SY	2449e8e5-9d7e-4119-9e7a-378efe55f875	19

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
49406-004-30	49406000430	1 TUBE in 1 BOX (49406-004-30) > 30 mL in 1 TUBE	1 tube	2020-07-13	0000-00-00	No	No	Current
49406-004-75	49406000475	1 BOTTLE in 1 BOX (49406-004-75) / 75 mL in 1 BOTTLE	1 bottle	2020-07-13	0000-00-00	No	No	Current