Breeze
FDA Label NDC 74955-028
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Cosmolive Kozmetik Sanayi Ve Ticaret Anonim Sirketi for the product Breeze (NDC 74955-028). 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 drug facts, active ingredient, purpose, warnings, otc - keep out of reach of children, directions, inactive ingredients, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl Alcohol 70%
Purpose
Antibacterial
Warnings
For external use only
Do not use if you are allergic to any of the ingredients
Keep pack tightly closed when not in use
Store in a cool and dry place
When using this product do not get into eyes. If contact occurs, rinse thoroughly with water.
Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
• Adults and children 2 years and over
• Apply to hands
• Allow to dry without wiping
• Do not flush
• Use the open product in 3 months
Inactive Ingredients
Waters, Glycerin, Aloe Barbadensis Leaf Juice, Tocopheryl acetate, Fragrance.
Packaging
Image (7495502801lb)
* Please review the disclaimer below.
