Active Ingredient
Alcohol 70%
Hand Sanitizer
FDA Label NDC 76383-020
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bbc Group Limited for the product Hand Sanitizer (NDC 76383-020). 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, use, warnings, do not use, when using this product, stop use and ask a doctor if, 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
Use
■ Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available
Warnings
For external use only. Flammable, keep away from fire and 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, and mouth. In case of contact with eyes, rinse eyes throughly wiyh water.
Stop Use And Ask A Doctor If
irritation and redness develops and persists.
Keep Out Of Reach Of Children
if swallowed, contact a doctor or Poison Control Center right away.
Directions
■ Apply a dime sized amount to hands. Rub hands together until dry ■ Supervise children under 6 years of age when using this product to avoid swallowing
Other Information
Store between 59-86°F. Avoid freezing and excessive heat above 104°F
Inactive Ingredients
Water, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Fragrance, Triethanolamine, Aloe Barbadensis Extract, Tocopheryl Acetate
Package Label
Package Label (Hrstylrhndsntzrlbl)
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