Active Ingredient
Active Ingredient:
Benzalkonium chloride 0.11 - 0.13%
Purpose
(sanitizing agent)
Sanaskin Hand And Body Sanitizer
FDA Label NDC 79637-120
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sanitin Products, Llc for the product Sanaskin Hand And Body Sanitizer (NDC 79637-120). 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 ingredient, purpose, directions, uses, warning, keep out of reach of children, inactive ingredients, sanaskin 275 gallon label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Purpose:
Sanitizing agent
Directions
Directions:
Apply directly to hands and rub thoroughly over desired areas. Continue rubbing until dry. Use frequently to avoid spreading germs.
Uses
Uses:
As a topical sanitizer. To help reduce the risk and spread of infection as well as communicable diseases by killing germs that reside on the surface of the skin.
Warning
Warning:
For external use only. do not use in eyes. In case of eye contact, immediately flush with water and seek medical advise. If swallowed, get medical help or contact poison control center right away. Discontinue use if skin irritation or redness develops. Not for use on sensitive areas of the body or burns. Keep out of reach of children
Keep Out Of Reach Of Children
Keep out of reach of children
Inactive Ingredients
Inactive ingredients: Water 99.83%, carbamide 0.04%
* Please review the disclaimer below.
