Dalan Ocean Breeze Antibacterial Deodorant
FDA Label NDC 51209-003

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Dalan Kimya Endustri A.s. for the product Dalan Ocean Breeze Antibacterial Deodorant (NDC 51209-003). 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 otc - purpose, uses, warnings, otc - keep out of reach of children, directions, inactive ingredients:, representative labeling, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Purpose

Triclosan 0.1% ...... Antibacterial

Uses

Antibacterial Soap

Warnings

For external use only
Do not use

  • this product on infants under 6 months of age.
  • in the eyes. If contact occurs, flush eyes with water.

    • Stop use and ask a doctor if irritation and redness develops or if condition persists 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

Lather over wet skin and rinse well

Inactive Ingredients:

Sodium Tallowate, Sodium Palmate, Water (Aqua), Sodium Palm Kernelate, Fragrance, Sodium Chloride, Alkyl Lactate, Propylene Glycol, Potassium Iodide, Fucus Vesiculosus Extract, Titanium Dioxide, Etidronic Acid, Linalool, Limonene, Sodium Benzoate, Potassium Sorbate.

Representative Labeling

Oceanbreeze90glabel (Oceanbreeze90glabel)

Oceanbreeze90glabel (Oceanbreeze90glabel)

Oceanbreeze125glabel (Oceanbreeze125glabel)

Oceanbreeze125glabel (Oceanbreeze125glabel)

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