Active Ingedient
Benzalkonium Chloride 0.13%
Sanitx Wet Wipes
FDA Label NDC 78822-100
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sanita Persona Sal for the product Sanitx Wet Wipes (NDC 78822-100). 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 ingedient, purpose, uses, warnings, keep out of reach of children, directions, inactive ingredients, sanitx wet wipes, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Uses
Hand sanitizer to help reduce bacteria on the skin
Warnings
For external use only
Do not use if you are allergic to any of the ingredients
When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. avoid contact with broken, irritated, or itching skin.
Stop use and ask a doctor if irritation or redness develops and the condition persists for more than 72 hours.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
Directions
- Wet hands thoroughly with product and allow to dry
- Discard wipe in a trash receptacle after use. Do not flush.
- Children under 6 years of age should be supervised.
Inactive Ingredients
Aqua, Propylene glycol, Polyquaternium-7, Phenoxyethanol, PEG-7 Glyceryl Cocoate, Polysorbate-20, Parfum, Aloe Barbadensis Leaf Extract, Urea, Ethylenediaminetetraacetic acid, Tetrasodium salt, Ethylhexylglycerin, Methylisothiazolinone
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