URBAN STREET OCEAN BREEZE- ocean breeze roll on antiperspirant/deodorant stick

Urban Street Ocean Breeze by

Drug Labeling and Warnings

Urban Street Ocean Breeze by is a Otc medication manufactured, distributed, or labeled by Blue Cross Laboratories LLC, Blue Cross Laboratories. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Aluminum Chloride 25.0%

Purpose

Antiperspirant

Use

Reduces underarm perspiration. Extra effective

Warnings

For external use only

Do not use on broken skin.

Stop use and ask a doctor if rash or irritation occurs

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

Ask a doctor before use if you have kidney disease.

Directions

Apply to underarms only.

Inactive Ingredients:

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

INDICATIONS & USAGE

PRINCIPAL DISPLAY PANEL

Urban Street

Ocean Breeze

Roll On

Antiperspirant/Deodorant

3.25 fl. oz. (96.1 ml)

INGREDIENTS AND APPEARANCE

URBAN STREET OCEAN BREEZE 
ocean breeze roll on antiperspirant/deodorant stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 22431-227
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B)	ALUMINUM CHLORIDE	250 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
STEARETH-21 (UNII: 53J3F32P58)
PPG-15 STEARYL ETHER (UNII: 1II18XLS1L)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)
WATER (UNII: 059QF0KO0R)
STEARETH-2 (UNII: V56DFE46J5)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22431-227-01	9.6 g in 1 TUBE; Type 0: Not a Combination Product	07/19/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	07/19/2021

Labeler - Blue Cross Laboratories LLC (008298879)

Registrant - Blue Cross Laboratories LLC (008298879)

Establishment
Name	Address	ID/FEI	Business Operations
Blue Cross Laboratories		008298879	manufacture(22431-227)