Active Ingredient
Aluminum Chloride 25.0%
Urban Street Ocean Breeze
FDA Label NDC 22431-227
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Blue Cross Laboratories Llc for the product Urban Street Ocean Breeze (NDC 22431-227). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, use, warnings, otc - do not use, otc - stop use, otc - keep out of reach of children, otc - ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiperspirant
Use
Reduces underarm perspiration. Extra effective
Warnings
For external use only
Otc - Do Not Use
Do not use on broken skin.
Otc - Stop Use
Stop use and ask a doctor if rash or irritation occurs
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact poison control center right away.
Otc - Ask Doctor
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
Package Label.Principal Display Panel
Urban Street
Ocean Breeze
Roll On
Antiperspirant/Deodorant
3.25 fl. oz. (96.1 ml)
* Please review the disclaimer below.
