FDA.reportPublic FDA data

TOENAIL FUNGUS TREATMENT MAXIMUM STRENGTH Liquid

Product NDC
84614-002
11-digit product format
846140002
Labeler code
84614
Product ID
84614-002_48b9ae23-4075-7b2c-e063-6294a90a27e6
Type
HUMAN OTC DRUG
Nonproprietary name
Tolnaftate
Dosage form
LIQUID
Route
TOPICAL
Labeler
Shenzhen Ctrip Technology Co., Ltd.
Application
M005
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-08-23
Substance
TOLNAFTATE
Active strength
1 g/100mL
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 · 2 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-08-27 00:01 UTC · source 2025-08-26excluded productproduct84614-002IInactivated by FDAexcluded / ndc_excluded.zipf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage84614-00284614-002-01IInactivated by FDAexcluded / ndc_excluded.zipf5e01cc5f278…a2eaf40c39c3…

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
TOENAIL FUNGUS TREATMENT MAXIMUM STRENGTH Liquid
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
TOLNAFTATE1 g/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
06KB629TKVInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
313423Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1fb03184-5f21-c82a-e063-6294a90a9fa4Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84614-002-012025-09-12C16284748780-13b156c62-2dd7-fb37-e063-e6dba90a4e0784614-002 TOENAIL FUNGUS TREATMENT MAXIMUM STRENGTH Liquid
84614-002-012025-07-29C16284748780-13b156c62-2dd7-fb37-e063-e6dba90a4e0784614-002 TOENAIL FUNGUS TREATMENT MAXIMUM STRENGTH Liquid

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84614-002-01TOENAIL FUNGUS TREATMENT MAXIMUM STRENGTH Liquid2 in 1 PACKAGELIQUID22
84614-002-01TOENAIL FUNGUS TREATMENT MAXIMUM STRENGTH Liquid30 mL in 1 BOTTLELIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84614-002TOENAIL FUNGUS TREATMENT MAXIMUM STRENGTH LIQUID (TOLNAFTATE) LIQUID [SHENZHEN CTRIP TECHNOLOGY CO., LTD.]1Current NDC, 2 package rows20240824_1fb03184-5f21-c82a-e063-6294a90a9fa4.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 11 of 49 · 973 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Miconazole NitrateATHLETES FOOT POWDER SPRAY TALC FREEChain Drug Marketing Association327095bd-a7c9-291d-e063-6394a90afafa2026-06-09WarningsExact identifier
application number: M005
TolnaftateANTIFUNGAL LIQUID SPRAYChain Drug Marketing Association34b5c11f-710f-60e4-e063-6394a90a990d2026-06-09WarningsExact identifier
application number: M005
TolnafateTOLNAFTATE POWDER SPRAYChain Drug Marketing Association342affe8-0a4d-6fe6-e063-6394a90a8dad2026-06-09WarningsExact identifier
application number: M005
Miconazole NitrateATHLETES FOOT POWDER SPRAY TALC FREEChain Drug Marketing Associationedc2da26-ae46-4175-86ed-83e1a65f6d142026-06-09WarningsExact identifier
application number: M005
TolnaftateANTIFUNGAL LIQUID SPRAYChain Drug Marketing Associationaa97d2ca-bcf4-3ee1-e053-2a95a90a748d2026-06-09WarningsExact identifier
application number: M005
TolnafateTOLNAFTATE POWDER SPRAYChain Drug Marketing Association1bd8e096-1717-4656-b52c-086d2f56f0702026-06-09WarningsExact identifier
application number: M005
BODYKOO JOCK ITCH CreamCLOTRIMAZOLE1% JOCK ITCH CREAMJiangxi Yudexi Pharmaceutical Co., LTD53553b31-81bb-d293-e063-6294a90aa0a52026-06-09WarningsExact identifier
application number: M005
BODYKOO ATHLETE FOOT CreamMICONAZOLE NITRATE2% ATHLETE FOOT CREAMJiangxi Yudexi Pharmaceutical Co., LTD53561903-54fe-f8ec-e063-6294a90a19fe2026-06-09WarningsExact identifier
application number: M005
Clotrimazole CreamCLOTRIMAZOLE USP1%Aldermed Inc.53bdd76b-6290-f1d3-e063-6394a90a9ff12026-06-08WarningsExact identifier
application number: M005
Miconazole CreamMICONAZOLE NITRATEAldermed Inc.4a7fc48a-c103-dc84-e063-6394a90ab80f2026-06-08WarningsExact identifier
application number: M005
Antifungal PowderMICONAZOLE NITRATEAldermed Inc.60954089-5220-4f4c-8595-b5ee4562562c2026-06-08WarningsExact identifier
application number: M005
Jock Itch PowderMICONAZOLE NITRATEWalgreens Company06d2f36c-8615-af08-e063-6394a90aa4242026-06-05WarningsExact identifier
application number: M005
Miconazole Nitrate 2%JOCK ITCH SPRAYWalgreens Companycf6cbaf4-beba-6fdf-e053-2995a90a76d22026-06-04WarningsExact identifier
application number: M005
Charmpoo Antifungal CreamMICONAZOLE NITRATE 2% ANTIFUNGAL CREAMJiangxi Yudexi Pharmaceutical Co., LTD5368b131-7537-8679-e063-6394a90a67542026-06-04WarningsExact identifier
application number: M005
Nail Fungus Treatment PenUNDECYLENIC ACID, TOLNAFTATEGUANGZHOU SAWEILAN IMPORT & EXPORT TRADING CO., LTD3fe842e1-b3db-c003-e063-6394a90a46b82026-06-04WarningsExact identifier
application number: M005
Lasolex ACMICONAZOLE NITRATE 2% ANTIFUNGALPureTek Corporation52bb4bc1-e88f-f5ea-e063-6394a90ae1e82026-06-03WarningsExact identifier
application number: M005
ClotrimazoleCLOTRIMAZOLESun Pharmaceutical Industries, Inc.13a14d3c-bfce-42b5-8463-4ec69e94774e2026-06-03WarningsExact identifier
application number: M005
Kopa Haiku Antifungal CreamMICONAZOLE NITRATE 2%Trovina Co. Ltd43cbad59-9899-ab3b-e063-6294a90a9e122026-06-02WarningsExact identifier
application number: M005
Athletes Foot CreamCLOTRIMAZOLEShenzhen Miandou Technology Co.,Ltd.53451e74-719e-9499-e063-6394a90a9e5a2026-06-02WarningsExact identifier
application number: M005
Lasolex ALMICONAZOLE NITRATE 2% ANTIFUNGALPureTek Corporation534df9be-b47a-03a1-e063-6394a90a265a2026-06-02WarningsExact identifier
application number: M005

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
313423tolnaftate 1 % Topical SolutionPSN1fb03184-5f21-c82a-e063-6294a90a9fa42
313423tolnaftate 10 MG/ML Topical SolutionSCD1fb03184-5f21-c82a-e063-6294a90a9fa42
313423tolnaftate 1 % Topical SolutionSY1fb03184-5f21-c82a-e063-6294a90a9fa42

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
84614-002-01846140002012 BOTTLE in 1 PACKAGE (84614-002-01) / 30 mL in 1 BOTTLE2 bottle2024-08-23NoNoCurrent