Active Ingredient(S)
Alcohol 75%
Hand Sanitizer Gel
FDA Label NDC 80072-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Care + 1 Llc for the product Hand Sanitizer Gel (NDC 80072-003). 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(s), purpose, use, warnings, otc - when using, otc - stop use, otc - 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
Antimicrobial
Use
Hand Sanitizer to help reduce bacteria on the skin
Warnings
For external use only. Flammable. Keep away from heat or flame
Otc - When Using
When using this product
Avoid contact with face, eyes and broken skin. In case of contact with eyes, flush with plenty of water and seek medical advice.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center
Directions
- Wet hands thoroughly with product and rub into skin until dry.
- Children under 6 years of age should be supervised by an adult when using this product.
Inactive Ingredients
water (aqua), Aloe, Carbomer, Tocopheryl Acetate (Vitamin E), Trolamine
Hand Sanitizer Gel Bottle - 1 Fl Oz - 30 Ml
Hand Sanitizer Gel Bottle 1 FL OZ 30 ML
* Please review the disclaimer below.
