FDA.reportPublic FDA data

TIDL PAIN RELIEF NUMBING

Product NDC
79740-009
Requested package NDC
79740-009-01
11-digit product format
797400009
Labeler code
79740
Product ID
79740-009_e8152b5d-2613-109d-e053-2a95a90a8360
Type
HUMAN OTC DRUG
Nonproprietary name
PAIN RELIEF
Dosage form
PATCH
Route
TOPICAL
Labeler
The Anthos Group
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-08-31
Marketing end
0000-00-00
Substance
LIDOCAINE; MENTHOL
Active strength
4 g/1001; g/1001
Pharmacologic classes
Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

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
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage79740-00979740-009-01IInactivated by FDA2026-09-14

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
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage79740-00979740-009-01IInactivated by FDAexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage79740-00979740-009-01IInactivated by FDAexcluded / ndc_excluded.zipf5e01cc5f278…a2eaf40c39c3…

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
777d68c6-a5ab-e06c-d314-677b0b9af0c8Product name220240508
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79740-009-012025-07-29C16284748780-11030e365-3e4c-111a-e063-dadaa90a10e279740-009 更新信息 TIDL PAIN RELIEF NUMBING PATCH
79740-009-012024-02-21C16284748780-11030e365-3e4c-111a-e063-dadaa90a10e279740-009 更新信息 TIDL PAIN RELIEF NUMBING PATCH
79740-009-012024-01-30C16284748780-11030e365-3e4c-111a-e063-dadaa90a10e279740-009 更新信息 TIDL PAIN RELIEF NUMBING PATCH

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79740-009-01TIDL PAIN RELIEF NUMBINGTIDL5 in 1 BOXPATCH52
79740-009-02TIDL PAIN RELIEF NUMBINGTIDL1 in 1 BAGPATCH12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79740-009TIDL PAIN RELIEF NUMBING TIDL (PAIN RELIEF) PATCH [THE ANTHOS GROUP]2Legacy NDC, 2 package rows20240223_e815287d-d589-2854-e053-2a95a90ad940.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1649008lidocaine 4 % / menthol 3 % Medicated PatchPSNe815287d-d589-2854-e053-2a95a90ad9402
1649008lidocaine 0.04 MG/MG / menthol 0.03 MG/MG Medicated PatchSCDe815287d-d589-2854-e053-2a95a90ad9402
1649008lidocaine 4 % / menthol 3 % Medicated PatchSYe815287d-d589-2854-e053-2a95a90ad9402

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
79740-009-01797400009015 BAG in 1 BOX (79740-009-01) > 1 PATCH in 1 BAG (79740-009-02) 5 bag2020-08-310000-00-00NoNoCurrent