FDA.reportPublic FDA data

Personal CARE

Product NDC
72133-210
Requested package NDC
72133-210-08
11-digit product format
721330210
Labeler code
72133
Product ID
72133-210_6a37570e-c42d-d091-e053-2991aa0acbb9
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol
Dosage form
GEL
Route
TOPICAL
Labeler
Delta Brands & Products LLC
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2018-04-02
Marketing end
0000-00-00
Substance
MENTHOL
Active strength
1 g/100g
NDC exclude flag
No
Listing certified through
2020-12-31
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 packagepackage72133-21072133-210-08IInactivated 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 · 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 packagepackage72133-21072133-210-08IInactivated by FDAexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage72133-21072133-210-08IInactivated by FDAexcluded / ndc_excluded.zipf5e01cc5f278…a2eaf40c39c3…

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
72133-210-082025-07-29C16284748780-13b156c62-26a2-fb37-e063-e6dba90a4e076a37570e-c41b-d091-e053-2991aa0acbb9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72133-210-08Personal CAREICE COLD ANALGESIC227 g in 1 JARGEL2271

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72133-210PERSONAL CARE ICE COLD ANALGESIC (MENTHOL) GEL [DELTA BRANDS & PRODUCTS LLC]1Legacy NDC, 1 package rows20180419_6a37570e-c41b-d091-e053-2991aa0acbb9.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
866128menthol 1.25 % Topical GelPSN6a37570e-c41b-d091-e053-2991aa0acbb91
866128menthol 0.0125 MG/MG Topical GelSCD6a37570e-c41b-d091-e053-2991aa0acbb91
866128menthol 1.25 % Topical GelSY6a37570e-c41b-d091-e053-2991aa0acbb91

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72133-210-0872133021008227 g in 1 JAR (72133-210-08) 227 g2018-04-020000-00-00NoNoCurrent