sting relief medicated pad

Product NDC
80514-005
11-digit product format
805140005
Labeler code
80514
Product ID
80514-005_ae73bcdd-ea3c-ed7d-e053-2a95a90a508d
Type
HUMAN OTC DRUG
Nonproprietary name
Benzocaine 6%, Isopropyl alcohol 60%
Dosage form
SWAB
Route
TOPICAL
Labeler
JIANGSU HAIDA INTERNATIONAL TRADING CO., LTD.
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-09-04
Marketing end
0000-00-00
Substance
BENZOCAINE; ISOPROPYL ALCOHOL
Active strength
6 g/100g; g/100g
NDC exclude flag
No
Listing certified through
2021-12-31
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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct80514-005IInactivated by FDA2026-10-05
excluded packagepackage80514-00580514-005-01IInactivated by FDA2026-10-05

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 · 18 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCCodeStatusSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductIInactivated by FDAd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage80514-005-01IInactivated by FDAd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductIInactivated by FDAf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage80514-005-01IInactivated by FDAf5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31excluded productproductIInactivated by FDA2ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-31excluded packagepackage80514-005-01IInactivated by FDA2ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28excluded productproductIInactivated by FDAa1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-28excluded packagepackage80514-005-01IInactivated by FDAa1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21excluded productproductIInactivated by FDAcfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-21excluded packagepackage80514-005-01IInactivated by FDAcfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10excluded productproductIInactivated by FDAcdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-10excluded packagepackage80514-005-01IInactivated by FDAcdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31excluded productproductUExcluded because listing certification expired302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-31excluded packagepackage80514-005-01UExcluded because listing certification expired302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20excluded productproductUExcluded because listing certification expireded331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-20excluded packagepackage80514-005-01UExcluded because listing certification expireded331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10excluded productproductUExcluded because listing certification expired0efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage80514-005-01UExcluded because listing certification expired0efc9e666f02…f202fb6c5f17…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80514-005-012025-01-30C16284748780-12cef2736-8c56-d83d-e063-dadaa90ab31fae737cf3-ff74-0b8f-e053-2a95a90a33ed

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80514-005-01sting relief medicated pad0.5 g in 1 POUCHSWAB0.52

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80514-005STING RELIEF MEDICATED PAD (BENZOCAINE 6%, ISOPROPYL ALCOHOL 60%) SWAB [JIANGSU HAIDA INTERNATIONAL TRADING CO., LTD.]2Legacy NDC, 1 package rows20231226_ae737cf3-ff74-0b8f-e053-2a95a90a33ed.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
895749benzocaine 6 % / isopropyl alcohol 60 % Medicated PadPSNae737cf3-ff74-0b8f-e053-2a95a90a33ed2
895749benzocaine 60 MG/ML / isopropyl alcohol 0.6 ML/ML Medicated PadSCDae737cf3-ff74-0b8f-e053-2a95a90a33ed2
895749benzocaine 6 % / isopropyl alcohol 60 % Medicated PadSYae737cf3-ff74-0b8f-e053-2a95a90a33ed2
895749benzocaine 6 % / isopropyl alcohol 60 % Topical SwabSYae737cf3-ff74-0b8f-e053-2a95a90a33ed2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
80514-005-0180514000501.5 g in 1 POUCH (80514-005-01) 2020-09-040000-00-00NoNoCurrent