4OZ MEDICATED CHEST RUB

Product NDC
81984-099
Requested package NDC
81984-099-01
11-digit product format
819840099
Labeler code
81984
Product ID
81984-099_60c0bc37-83b2-3280-e053-2a91aa0ae7c9
Type
HUMAN OTC DRUG
Nonproprietary name
menthol, camphor, eucalyptus oil
Dosage form
OINTMENT
Route
TOPICAL
Labeler
Pride Products Corporation
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2017-12-01
Marketing end
0000-00-00
Substance
MENTHOL; EUCALYPTUS OIL; CAMPHOR (SYNTHETIC)
Active strength
1 g/100g; g/100g; 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 packagepackage81984-09981984-099-01IInactivated by FDA2026-10-12

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…

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
81984-099-012025-01-30C16284748780-12cef2736-b0ff-d83d-e063-dadaa90ab31f60c0bc37-83b1-3280-e053-2a91aa0ae7c9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81984-099-014OZ MEDICATED CHEST RUB110 g in 1 JAROINTMENT1101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81984-0994OZ MEDICATED CHEST RUB (MENTHOL, CAMPHOR, EUCALYPTUS OIL) OINTMENT [PRIDE PRODUCTS CORPORATION]1Legacy NDC, 1 package rows20171222_60c0bc37-83b1-3280-e053-2a91aa0ae7c9.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1042786camphor 4.7 % / eucalyptus oil 1 % / menthol 1 % Topical OintmentPSN60c0bc37-83b1-3280-e053-2a91aa0ae7c91
1042786camphor 0.047 MG/MG / Eucalyptus oil 0.01 MG/MG / menthol 0.01 MG/MG Topical OintmentSCD60c0bc37-83b1-3280-e053-2a91aa0ae7c91
1042786camphor 4.7 % / eucalyptus oil 1 % / menthol 1 % Topical OintmentSY60c0bc37-83b1-3280-e053-2a91aa0ae7c91

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
81984-099-0181984009901110 g in 1 JAR (81984-099-01) 110 g2017-12-010000-00-00NoNoCurrent