FDA.reportPublic FDA data

Urban Street Ocean Breeze

Manufacturer
Blue Cross Laboratories LLC | Blue Cross Laboratories
Effective date
2021-07-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:41:35

Label at a glance#

ProductUrban Street Ocean Breeze
Active ingredientALUMINUM CHLORIDE
Label structure7 sections

Dosage and administration

Apply to underarms only.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chloride 25.0%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

Reduces underarm perspiration. Extra effective

Warnings

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use on broken skin.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash or irritation occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact poison control center right away.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have kidney disease.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to underarms only.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, Steareth-2, Steareth-31, Fragrance, PPF-15 Stearyl Ether, Phenoxyethanol, Aluminum Starch Octenylsuccinate, Isopropyl Myristate, Methylisothiazolinone

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Urban Street Ocean BreezeUrban Street Ocean BreezeUrban Street

Ocean Breeze

Roll On

Antiperspirant/Deodorant

3.25 fl. oz. (96.1 ml)

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

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
22431-22722431-227-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
STEARETH-2153J3F32P58IACT
PPG-15 STEARYL ETHER1II18XLS1LIACT
PHENOXYETHANOLHIE492ZZ3TIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
FRAGRANCE CLEAN ORC0600327329LCV5BTFIACT
WATER059QF0KO0RIACT
ALUMINUM CHLORIDE3CYT62D3GAACTIB
STEARETH-2V56DFE46J5IACT
ALUMINUM STARCH OCTENYLSUCCINATEI9PJ0O6294IACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c69de587-de0c-8acc-e053-2a95a90ad56dc69de587-de0b-8acc-e053-2a95a90ad56d2021-07-08WarningsExact identifier
spl id: c69de587-de0c-8acc-e053-2a95a90ad56d
spl set id: c69de587-de0b-8acc-e053-2a95a90ad56d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.