Otc - When Using
Benzalkonium chloride 0.13 %
Seratin
FDA Label NDC 79652-011
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Vernel Kozmetik Sanayi Ve Ticaret Anonim Sirketi for the product Seratin (NDC 79652-011). 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 - when using, otc - purpose, warnings, otc - active ingredient, otc - stop use, otc - keep out of reach of children, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Antibacterial
Warnings
For external use only ; only hands
Otc - Active Ingredient
avoid contact with eyes.If contact occurs , rinse eyes thoroughly with water
antimicrobial
Otc - Stop Use
- irritation or redness develops
- condition persists for more than 72 hours
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away
Inactive Ingredient
glycerin, sodium laureth sulfate, lauramine oxide, cocamidopropyl betaine, edetate sodium, water, citric acid monohydrate, polyquaternium-7,aloe vera leaf,cocamide, cetrimonium chloride,methylchloroisothiazolinone,styrene/ acrylamide copolymer, fragrance lavender& chia F-153480, alpha-tocopherol acetate, sodium chloride
Package Label.Principal Display Panel
Seratin Antibacterial Soap 450 mL Back (Seratin 450ml Back)
Seratin Antibacterial Soap 450 mL Front (Seratin 450ml Front)
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