Otc - Active Ingredient
Active Ingredient
Ethyl Alcohol 62%
Clean Hand Sanitizer
FDA Label NDC 58180-210
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bicooya Cosmetics Limited for the product Clean Hand Sanitizer (NDC 58180-210). 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, indications & usage, warnings, otc - when using, otc - keep out of reach of children, other, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
Antiseptic
Indications & Usage
Uses • sanitizer spray to help decrease bacteria on the skin
•recommended for repeated use.
Warnings
Warnings •Flammable. • Keep away from fire or flame. •For external use only
Otc - When Using
When using this product •avoid contact with eyes • in case of contact, rinse eyes throughtly with water
•do not apply around eyes, do not use near the eyes and mouth.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. if sweallowede, get medical help or contact a Poison Control Center right away.
Other
Other information • do not store above 105F. May discolor some fabrics.
Dosage & Administration
Directions • spray enough product in your palms and thoroughly spread on both hands and rub into skin until dry.
Inactive Ingredient
Inactive ingredients aloe barbadensis gel, carbomer, fragrance, FD&C blue no. 1, FD&C yellow no.5, glycerin, isopropyl alcohol, PEG-40 hydrogenated castor oil, propylene glycol, triethanolamine, water
Package Label.Principal Display Panel
Package Label
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