Active Ingredient
Ethyl Alcohol 75%
Hand Sanitizer
FDA Label NDC 76782-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Blue Mineral Corporation for the product Hand Sanitizer (NDC 76782-003). 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 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
Uses
• For hand sanitizing to decrease bacteria on the skin
• Recommended for repeated use
Warnings
For external use only
When Using This Product:
avoid contact with eyes. In case of eye contact, flush eyes with water.
Stop Use And Ask A Doctor If:
irritation or redness develops, or if condition persists for more than 72 hours.
Keep Out Of Reach Of Children:
If swallowed get medical help or contact a Poison Control Center right away.
Directions:
Squeeze appropriate amount sanitizer on to hands and rub together until dry. Use as needed. For children under 6, use with adult supervision. Not recommended for infants.
Inactive Ingredients:
Water (Aqua),Aloe Barbadensis leaf Extract. Acrylates/C10-30 alkyl Acrylate Crosspolymer, Tetrahydroxypropyl Ethylenediamine
* Please review the disclaimer below.
