FDA.reportPublic FDA data

Foot Cure Antifungal Foot Balm

Product NDC
83691-010
11-digit product format
836910010
Labeler code
83691
Product ID
83691-010_770b31d7-de25-4a4e-85d3-1e2d9a84c9bd
Type
HUMAN OTC DRUG
Nonproprietary name
ZINC UNDECYLENATE
Dosage form
OINTMENT
Route
TOPICAL
Labeler
Sansar LLC
Application
M005
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-06-30
Substance
ZINC UNDECYLENATE
Active strength
10 g/100g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

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
Foot Cure Antifungal Foot Balm
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ZINC UNDECYLENATE10 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
388VZ25DURInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
2712154Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
ac6075bf-cc1d-4e8a-aa13-5a85e80f34eeAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83691-010-01Foot Cure Antifungal Foot Balm57 g in 1 BOTTLEOINTMENT572
83691-010-01Foot Cure Antifungal Foot Balm1 in 1 BOXOINTMENT12
83691-010-02Foot Cure Antifungal Foot Balm2 in 1 BOXOINTMENT22
83691-010-02Foot Cure Antifungal Foot Balm57 g in 1 BOTTLEOINTMENT572

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83691-010FOOT CURE ANTIFUNGAL FOOT BALM (ZINC UNDECYLENATE) OINTMENT [SANSAR LLC]1Current NDC, 4 package rows20250419_ac6075bf-cc1d-4e8a-aa13-5a85e80f34ee.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 29 of 49 · 969 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MedlineMICONAZOL NITRATEMedline Industries, LPdad58efb-cc20-577a-e053-2a95a90abd9d2025-11-03WarningsExact identifier
application number: M005
TolnafateTOLNAFTATE POWDER SPRAYHEBc6af941a-0b85-4611-a6f3-b13fcf3c4a872025-11-03WarningsExact identifier
application number: M005
TolnaftateFOOT ODOR CONTROL SPRAYHEBc585605b-ecb8-4dd8-9205-a9be02d751fa2025-11-03WarningsExact identifier
application number: M005
Premier Solutions Antifungal Tolnaftate LiquidTOLNAFTATEPremier Brands of America, Inc.e1971c1c-5687-577b-e053-2a95a90ad95f2025-11-03WarningsExact identifier
application number: M005
Miconazole nitrateANTIFUNGAL MICONAZOLE LIQUID CONTINUOUS SPRAYPremier Brands of America Inc.3803c643-35d1-06d4-e063-6294a90ac6f62025-11-03WarningsExact identifier
application number: M005
Anti-fungal Powder Miconazole NitrateMICONAZOLE NITRATEMeijer Distribution Inc03fd069d-685d-b8ac-e063-6394a90a31f82025-10-31WarningsExact identifier
application number: M005
TolnaftateANTIFUNGAL LIQUID SPRAYPremier Brands of America Inc.7a6a63cd-e87d-4229-8acf-b65d63909eb62025-10-31WarningsExact identifier
application number: M005
AzolenMICONAZOLE NITRATEStratus Pharmaceuticals, Inc.9c2574f3-3be4-405a-9c87-943dc6ef87772025-10-30WarningsExact identifier
application number: M005
Family Care AntifungalCLOTRIMAZOLEUnited Exchange Corp.63255079-ecf1-1e77-e053-2a91aa0a7b6c2025-10-30WarningsExact identifier
application number: M005
Miconazorb AFMICONAZOLE NITRATEAmerisourceBergen Drug Corporation13a20d21-42d5-fe56-e063-6394a90aaf572025-10-30WarningsExact identifier
application number: M005
Antifungal Liquid ContinuousMICONAZOLE NITRATEFamily Dollar Services, Inc17cc4601-f946-df8b-e063-6394a90a38972025-10-30WarningsExact identifier
application number: M005
TolnaftateANTIFUNGAL LIQUID SPRAYARMY & AIR FORCE EXCHANGE SERVICE932b1be8-3dbb-49ae-822a-c44a24fbe36a2025-10-30WarningsExact identifier
application number: M005
Miconazole nitrateANTIFUNGAL MICONAZOLE LIQUID CONTINUOUS SPRAYGEISS, DESTIN AND DUNN, INC.c367c2e8-5423-bf01-e053-2a95a90ab8e92025-10-30WarningsExact identifier
application number: M005
Miconazole NitrateJOCK ITCH SPRAYHarris Teeter, LLC636b0d6f-4e36-4c96-9e71-7bfdebb7f3cb2025-10-30WarningsExact identifier
application number: M005
TolnaftateANTIFUNGAL LIQUID SPRAYHarris Teeter, LLCf140e9bb-507b-4048-8b7b-8cc51b6a497d2025-10-30WarningsExact identifier
application number: M005
HEB Athlete Foot AntifungalMICONAZOLE NITRATEHEB2e204111-b5d3-0220-e063-6294a90a67bb2025-10-30WarningsExact identifier
application number: M005
TolnaftateANTIFUNGAL SPRAY LIQUIDKroger Co.0cfebac3-684d-4599-b75f-9a82708db7172025-10-30WarningsExact identifier
application number: M005
Miconazole NitrateJOCK ITCH SPRAYKroger Co.86bdf8a6-3a1f-457b-e053-2991aa0a58102025-10-30WarningsExact identifier
application number: M005
TolnaftateTOLNAFTATE POWDER SPRAYKroger Co.f5c8dccd-8e69-6a01-e053-2a95a90a69722025-10-30WarningsExact identifier
application number: M005
TolnafateFOOT AND SNEAKER SPRAYKroger Co.72243b08-47cf-4db3-b834-b762b7f0ccf92025-10-30WarningsExact identifier
application number: M005

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2712154zinc undecylenate 10 % Topical OintmentPSNac6075bf-cc1d-4e8a-aa13-5a85e80f34ee2
2712154zinc undecylenate 0.1 MG/MG Topical OintmentSCDac6075bf-cc1d-4e8a-aa13-5a85e80f34ee2
2712154zinc undecylenate 10 % Topical OintmentSYac6075bf-cc1d-4e8a-aa13-5a85e80f34ee2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
83691-010-01836910010011 BOTTLE in 1 BOX (83691-010-01) / 57 g in 1 BOTTLE1 bottle2024-06-30NoNoCurrent
83691-010-02836910010022 BOTTLE in 1 BOX (83691-010-02) / 57 g in 1 BOTTLE2 bottle2024-06-30NoNoCurrent