Urban Street Ocean Breeze

Product NDC
22431-227
11-digit product format
224310227
Labeler code
22431
Product ID
22431-227_c69de587-de0c-8acc-e053-2a95a90ad56d
Type
HUMAN OTC DRUG
Nonproprietary name
Ocean Breeze Roll On Antiperspirant/Deodorant
Dosage form
STICK
Route
TOPICAL
Labeler
Blue Cross Laboratories LLC
Application
part350
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2021-07-19
Marketing end
0000-00-00
Substance
ALUMINUM CHLORIDE
Active strength
250 mg/g
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
22431-227-012022-07-29C16284748780-1e4f33bdf-a431-d8a0-e053-dadaa90a6e4ec69de587-de0b-8acc-e053-2a95a90ad56d

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
22431-227-01Urban Street Ocean Breeze9.6 g in 1 TUBESTICK9.61

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
22431-227URBAN STREET OCEAN BREEZE (OCEAN BREEZE ROLL ON ANTIPERSPIRANT/DEODORANT) STICK [BLUE CROSS LABORATORIES LLC]1Legacy NDC, 1 package rows20210720_c69de587-de0b-8acc-e053-2a95a90ad56d.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
22431-227-01224310227019.6 g in 1 TUBE (22431-227-01) 9.6 g2021-07-190000-00-00NoNoCurrent