Breeze Antibacterial 150 Ml
FDA Label NDC 74955-022

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 Antibacterial 150 Ml (NDC 74955-022). 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 for use, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredient

Ethanol 85%

Purpose

Antiseptic

Warnings

Flammable. Keep away from fire or flame.

For external use only

  • Avoid contact with eyes. In case of eye contact, rinse with water.
  • If irritation develops, discontinue use. Consult a doctor if irritation persists more than 72 hours.
  • Store in cool and dry place.

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children

Directions For Use

  • Hold the container 15 cm away.
  • Spray directly on hands and rub in thoroughly. Allow to dry.
  • Children under 6 years of age should be supervised when using BREEZE.

Other Information

  • Store between 68°F (20°C).
  • May discolor certain fabrics and surfaces.

Inactive Ingredients

  • Butane, Aqua, Propane, Isobutane, Propylene Glycol, Isopropyl Myristate, Parfum, Benzalkonium Chloride.

Packaging

Image (Labelnew)

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