Active Ingredient
Alcohol 72.1 w/w
Alsoft W Hand Sanitizer
FDA Label NDC 59900-351
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Best Sanitizers, Inc for the product Alsoft W Hand Sanitizer (NDC 59900-351). 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, uses, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Hand Sanitizer
Uses
- sanitizes hands to help reduce bacteria that potentially can cause disease
- helps to prevent cross-contamination
- recommended for repeated use
- helps pevent drying of skin
Warnings
- For external use only
- Flammable, keep away from fire or flame
Otc - When Using
When using this product
- do not use in or near eyes
- use in a well-ventilated area
Otc - Stop Use
Stop use and consult a doctor if irritation or redness develop.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
If swallowed, seek medical attention or contact Poison Control Center immediately.
Directions
- wet hands thoroughly with product, covering entire surface of hands, especially the fingernails and cuticles
- rub hands together until dry
Other Information
store in a cool, dry place below 104 F (40 C)
Inactive Ingredients
Carbomer, Glycerin, Glyceryl Caprate, Isopropyl Myristate, Tocopherol Acetate, Triethanolamine, Water
Questions?
Contact Best Sanitizers at 888-225-3267 Mon-Fri 9 am - 4 pm PST
Package Label.Principal Display Panel
Alsoft W
hand sanitizer gel
72.1%
Ethyl Alcohol
Net Contents: 16.9 fl oz (500 mL)
* Please review the disclaimer below.
