Active Ingredient
Alcohol 75%v/v
Hand Sanitizer
FDA Label NDC 80230-004
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Skymall Holdings Llc for the product Hand Sanitizer (NDC 80230-004). 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, do not use, when using this product, stop use and ask a doctor, keep out of reach of children, 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. For use when soap and water are not available.
Warnings
■ For external use only. Flammable. Keep away from heat or flame
Do Not Use
■ on children less than 2 months of age ■ on open skin wounds
When Using This Product
keep out of eyes, ears, ears and mouth. In case of eye contact immediately flush eyes thoroughly with water
Stop Use And Ask A Doctor
if irritation or rash occurs. These may be the signs of a serious condition.
Keep Out Of Reach Of Children
In case of accidentail ingestion, contact a doctor or Poison Control Center immediately.
Directions
■ Place enough product on hands to cover all surfaces. Rub hands together until dry. ■ Supervise children under 6 years of age when using this product to avoid swallowing.
Other Information
■ Store between 15°-30°C (59°-89°F) ■ Avoid freezing and excessive heat above 40°C (104°F) ■ May discolor fabrics or surfaces.
Inactive Ingredients
FD&C Blue 1, FD&C Yellow 5, Glycerin, Hydroxypropyl Cellulose, Water
Inner Package Label
Inner Package Label (2ozinnrhndsntzrgrn)
Outer Package Label
Outer Package Label (4x2hndsntzrpck)
Outer Package Label (8x2hndsntzrpck)
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