FDA.reportPublic FDA data

Odorono

Product NDC
51048-202
11-digit product format
510480202
Labeler code
51048
Product ID
51048-202_2c80c6dc-485c-4847-b5b8-a39d9ab74563
Type
HUMAN OTC DRUG
Nonproprietary name
Aluminum Chlorohydrate
Dosage form
LIQUID
Route
TOPICAL
Labeler
Omega & Delta Co
Application
part350
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2006-05-08
Marketing end
0000-00-00
Substance
ALUMINUM CHLOROHYDRATE
Active strength
20 g/100mL
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 productproduct51048-202IInactivated by FDA2026-10-15
excluded packagepackage51048-20251048-202-25IInactivated by FDA2026-10-15

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
2020-06-10 20:45 UTC · source 2020-06-10excluded productproduct51048-202IInactivated by FDAexcluded / ndc_excluded.zip9bebd1f3094a…5416666fcb17…
2020-06-10 20:45 UTC · source 2020-06-10excluded packagepackage51048-20251048-202-25IInactivated by FDAexcluded / ndc_excluded.zip9bebd1f3094a…5416666fcb17…

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
51048-202-252020-11-12C16284748780-19d75b9d0-5122-f424-e053-dadaa90a57ceOdorono Antiperspirant Deodorant Roll-on Powder
51048-202-252020-01-31C16284748780-19d75b9d0-5122-f424-e053-dadaa90a57ceOdorono Antiperspirant Deodorant Roll-on Powder

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51048-202-25OdoronoAntiperspirant and Deodorant Roll-on Powder74 mL in 1 BOTTLE, WITH APPLICATORLIQUID743

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51048-202ODORONO ANTIPERSPIRANT AND DEODORANT ROLL-ON POWDER (ALUMINUM CHLOROHYDRATE) LIQUID [OMEGA & DELTA CO]3Legacy NDC, 1 package rows20241121_38d4f89f-01c6-499c-8687-010a0dabc1c8.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
51048-202-255104802022574 mL in 1 BOTTLE, WITH APPLICATOR (51048-202-25) 74 ml2006-05-080000-00-00NoNoCurrent