Vaporizing Chest Rub

Product NDC
52000-039
Requested package NDC
52000-039-10
11-digit product format
520000039
Labeler code
52000
Product ID
52000-039_d8874472-8be1-38bc-e053-2995a90aaf3f
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol and Camphor and Eucalyptus Oil
Dosage form
GEL
Route
TOPICAL
Labeler
Universal Distribution Center LLC
Application
part341
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2018-05-14
Marketing end
0000-00-00
Substance
CAMPHOR (SYNTHETIC); EUCALYPTUS OIL; MENTHOL
Active strength
5 g/100g; g/100g; g/100g
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 packagepackage52000-03952000-039-10IInactivated 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 packagepackage52000-03952000-039-10IInactivated by FDAexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage52000-03952000-039-10IInactivated 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#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52000-039-08Vaporizing Chest Rub50 g in 1 BOTTLE, PLASTICGEL504
52000-039-09Vaporizing Chest Rub56.6 g in 1 BOTTLE, PLASTICGEL56.64
52000-039-10Vaporizing Chest Rub100 g in 1 BOTTLE, PLASTICGEL1004
52000-039-11Vaporizing Chest Rub113 g in 1 BOTTLE, PLASTICGEL1134
52000-039-12Vaporizing Chest Rub150 g in 1 BOTTLE, PLASTICGEL1504
52000-039-13Vaporizing Chest Rub170 g in 1 BOTTLE, PLASTICGEL1704
52000-039-14Vaporizing Chest Rub226 g in 1 BOTTLE, PLASTICGEL2264

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52000-039VAPORIZING CHEST RUB (MENTHOL AND CAMPHOR AND EUCALYPTUS OIL) GEL [UNIVERSAL DISTRIBUTION CENTER LLC]4Legacy NDC, 7 package rows20241212_cfec7539-8db6-4bdf-9a6b-3416e9afc6d9.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2045202camphor 4.7 % / eucalyptus oil 1.2 % / menthol 1.25 % Topical GelPSNcfec7539-8db6-4bdf-9a6b-3416e9afc6d94
2045202camphor 0.047 MG/MG / Eucalyptus oil 0.012 MG/MG / menthol 0.0125 MG/MG Topical GelSCDcfec7539-8db6-4bdf-9a6b-3416e9afc6d94
2045202camphor 4.7 % / eucalyptus oil 1.2 % / menthol 1.25 % Topical GelSYcfec7539-8db6-4bdf-9a6b-3416e9afc6d94

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
52000-039-1052000003910100 g in 1 BOTTLE, PLASTIC (52000-039-10) 100 g2018-05-140000-00-00NoNoCurrent