Active Ingredients
Alcohol 62% v/v
Hand Sanitizer
FDA Label NDC 76750-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Global Marketing Products Llc for the product Hand Sanitizer (NDC 76750-002). 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 ingredients, purpose, use, warnings, when using this product, stop use and ask a 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
Use
■ hand sanitizer to help reduce bacteriaon the skin. For use when soap and water are not available.
Warnings
For external use only. Flammable. Keep away from heat or flame
When Using This Product
■ keep out of eyes, ears, and mouth. ■ in case of eye contact immediately flush eyes thoroughly with water.
Stop Use And Ask A Doctor If
■ irritation or redness develops ■ conditions persist for more than 72 hours
Keep Out Of Reach Of Children
In case of accidental ingestion, contact a doctor or Poison Control Center immediately.
Directions
■ Squeeze 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 (59-86F) ■ may discolor fabrics or surfaces
Inactive Ingredients
Water, Carbomer, Aminomethyl Propanol
Package Label
Package Label (Hndsntzr62alcglbmktbaoliprd)
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