FDA.reportPublic FDA data

MAX PAIN RELIEF

Product NDC
82707-101
Requested package NDC
82707-101-15
11-digit product format
827070101
Labeler code
82707
Product ID
82707-101_deb230e2-bfcd-ab51-e053-2995a90a3fea
Type
HUMAN OTC DRUG
Nonproprietary name
CAMPHOR, MENTHOL
Dosage form
CREAM
Route
TOPICAL
Labeler
PROVEDA
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2022-05-10
Marketing end
0000-00-00
Substance
CAMPHOR OIL; MENTHOL
Active strength
3 g/100mL; g/100mL
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 packagepackage82707-10182707-101-15IInactivated by FDA2026-08-11

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 · 9 matching rows.

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

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82707-101-112025-01-30C16284748780-12cef2736-a249-d83d-e063-dadaa90ab31fPROVEDA - MAX PAIN RELIEF CREAM (82707-101)
82707-101-152025-01-30C16284748780-12cef2736-a249-d83d-e063-dadaa90ab31fPROVEDA - MAX PAIN RELIEF CREAM (82707-101)
82707-101-512025-01-30C16284748780-12cef2736-a249-d83d-e063-dadaa90ab31fPROVEDA - MAX PAIN RELIEF CREAM (82707-101)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82707-101-11MAX PAIN RELIEF100 mL in 1 BOTTLECREAM1002
82707-101-15MAX PAIN RELIEF15 mL in 1 TUBECREAM152
82707-101-50MAX PAIN RELIEF50 mL in 1 TUBECREAM502
82707-101-51MAX PAIN RELIEF1 in 1 BOXCREAM12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82707-101MAX PAIN RELIEF (CAMPHOR, MENTHOL) CREAM [PROVEDA]2Legacy NDC, 4 package rows20230927_deb230e2-bfcc-ab51-e053-2995a90a3fea.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
82707-101-158270701011515 mL in 1 TUBE (82707-101-15) 15 ml2022-05-100000-00-00NoNoCurrent