Abutol Sanitizing Aloe Vera
FDA Label NDC 77418-803
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Atak Farma Kozmetik Ve Kimya Sanayi Ticaret Anonim Sirketi for the product Abutol Sanitizing Aloe Vera (NDC 77418-803). 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 drug facts, active ingredient, purpose, uses, warnings, otc - keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Benzalkonium chloride 0.13%
Purpose
Antiseptic
Uses
• Hand sanitizer to decrease bacteria on the skin
• Recommended for repeated use
• For use when soap and water are not available
Warnings
For external use only. Protect from the sunlight.
Do not use
• on children less than 2 months of age
• on open skin wounds
When using this product • Avoid use on/or around eyes, ears, mouth, broken/ irritated skin or large areas of body. In case of a contact with eyes, rinse thoroughly with water several minutes. do not inhale or ingest
Otc - Keep Out Of Reach Of Children
Stop out of reach of children
If swallowed get medical help or contact a Poison Control Center right away.
Directions
• Hold upright at 6-7 inches away from surface and spray evenly. Repeat application a necessary when using this product to avoid swallowing
Other Information
• store between 15-30 C (59-86F)
Inactive Ingredients
Aqua, FD&C Blue No.1, FD&C Red No.40, Glycerin, Parfum.
Packaging
Image (7741880310)
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