Active Ingredient
Ethyl alcohol 80% v/v
Perfect Advanced Hand Sanitizer
FDA Label NDC 73919-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Vast Enterprises for the product Perfect Advanced Hand Sanitizer (NDC 73919-001). 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, when using this product, stop use and ask doctor if, 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
Antiseptic
Uses
Hand sanitizer to help reduce bacteria on the skin that potentially can cause disease. For use when soap and water are not available.
Warnings
Flammable, keep away from fire or flame
For external use only
Do not use onchildren less than 2 months old or on open skin wounds.
When Using This Product
keep out of eye. In case of contact rinse eyes thoroughly with water
Stop Use And Ask Doctor If
irritation or rash appears. These may be signs of a serious condition.
Keep Out Of Reach Of Children.
If swallowed, get medical help right away or contact a Poison Control Center immediately.
Directions
Put enough product in the palm to cover your hand and rub hands together briskly until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.
Other Information
Store between 15 - 30˚C (59 - 86˚F)
Avoid freezeing and excessive heat above 40˚C (104˚F).
May discolor certain fabrics or surfaces.
Inactive Ingredient
Deionized Water, Isopropyl Alcohol, Glycol Alcohol, Acrylic Crosspolymer, Trolamine, Fragrance.
Product Label
Image Description (Label)
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