Active Ingredient
Alcohol 62%
Hand Sanitizer
FDA Label NDC 76383-015
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 76383-015). 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, 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
for handwashing to decrease bacteria on the skin, only when water is not available
Warnings
For external use only. Flammable, keep away from fire and flame
When Using This Product
■ do not get into eyes ■ if contact occurs; rinse eyes thoroughly with water
Stop Use And Ask A Doctor If
■ irritation and redness develop
Keep Out Of Reach Of Children
if swallowed, get medical help or Poison Control Center right away.
Directions
■ wet hands thoroughly with product and allow to dry without wiping
Other Information
■ Store below 105°F ■ May discolor some fabrics
Inactive Ingredients
Water, PEG-40 Hydrogenated Castor Oil, Fragrance, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Sodium Hydroxide, Denatonium Benzoate
Package Label
Package Label (K7hndsntzrlbl)
* Please review the disclaimer below.
