Home NDC 49406-004 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 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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength 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 Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded 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 8 of 49 · 973 matching rows.
DailyMed RxNorm Mappings# 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