Active Ingredient(S)
Benzalkonium Chloride %0.13....Purpose: Antibacterial
Dex
FDA Label NDC 76964-300
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Tat Kimya Sabun Ve Gliserin Sanayi Ve Ticaret Anonim Sirketi for the product Dex (NDC 76964-300). 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(s), purpose, use, warnings, do not use, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antibacterial, Liquid Soap
Use
It helps eliminate bacteria on hands.
Warnings
For external use only. When using this product, avoid contact with eyes. In case of contact, flush with water.
Do Not Use
If swallowed, get medical help or contact a Poison Control Center right away.
Otc - When Using
When using this product, avoid contact with eyes. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Otc - Stop Use
If swallowed, get medical help or contact a Poison Control Center right away.
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
- wash hands and rinse
Other Information
- Store between 15-30C (59-86F)
- Avoid freezing and excessive heat above 40C (104F)
Inactive Ingredients
Aqua, Lauramine Oxide, Cetrimonium Chloride, Glycerin, PEG - 150 Distearate, Fragrance, Citric Acid, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1(CI 42051)
Package Label - Principal Display Panel
500 mL Antibacterial Liquid Soap Ndc: 76964-300-01 (Antibac)
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