Active Ingredient(S)
ETHYL ALCOHOL 62%
Antibacterial Hand Sanitizer
FDA Label NDC 70445-411
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Webb Business Promotions, Incorporated for the product Antibacterial Hand Sanitizer (NDC 70445-411). 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(s), purpose, use, otc - keep out of reach of children, directions, other information, inactive ingredients, package label.principal display panel, 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 DECREASE BACTERIA ON THE SKIN. WHEN WATER, SOAP & TOWEL ARE NOT AVAILABLE. RECOMMENDED FOR REPEATED USE.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. Children must be supervised in use of this product.
Directions
SQUIRT AS NEEDED INTO PALMS AND THOROUGHLY SPREAD ON BOTH HANDS. RUB INTO SKIN UNTIL DRY.
Other Information
Store at 20°C (68°- 77°F). May discolor fabrics
Inactive Ingredients
WATER, PROPYLENE GLYCOL, CARBOMER, TRIETHANOLAMINE, FRAGRANCE, TOCOPHEROL, ALOE VERA
* Please review the disclaimer below.
