Otc - Active Ingredient
Active Ingredient(s): Ethyl Alcohol 68%
Hand Sanitizer Ocean Breeze
FDA Label NDC 54225-005
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Yiwu Sloggi Cosmetics Co.,ltd for the product Hand Sanitizer Ocean Breeze (NDC 54225-005). 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 - active ingredient, otc - purpose, dosage & administration, warnings, inactive ingredient, indications & usage, otc - keep out of reach of children, 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
Purpose: Antiseptic
Dosage & Administration
Place enough product on hands to cover all surfaces.
Warnings
For external use only.
Inactive Ingredient
Isopropyl Alcohol
Water
Triethanolamine
Fragrance
Indications & Usage
Rub hands together until dry.
Otc - Keep Out Of Reach Of Children
Keep away from children.
Package Label.Principal Display Panel
30mL Ocean Breeze NDC 54225-005-01
100mL Ocean Breeze NDC 54225-005-02
500mL Ocean Breeze NDC 54225-005-03
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