Active Ingredient
Ethyl Alcohol 70% .........................Antimicrobial
Andys
FDA Label NDC 73755-110
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Brand Name Distributors for the product Andys (NDC 73755-110). 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, directions and usd, inactive ingredients, warning, keep out of reach of children., purpose, dosage, andy's hand sanitizer unscented, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Directions And Usd
USE Hand Sanitizer to help reduce bacteria on the skin
INDICATION Put enough product in your palm to cover hands and rub hands together briskly until dry
Inactive Ingredients
Carbomer, Triethanolamine Lauryl Sulfate, water
Warning
Flammable. Keep away from fire or flame. For external use only. When using this product: Don't use in or near the eyes.
In the case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash appears and lasts.
Keep Out Of Reach Of Children.
Keep Out of Reach of Children. If swallowed, get medical help or contact poison control center right away
Purpose
Antimicrobial
Dosage
USE Hand Sanitizer to help reduce bacteria on the skin
INDICATION Put enough product in your palm to cover hands and rub hands together briskly until dry
Andy's Hand Sanitizer Unscented
Kills Over 99% of Most Common Germs
Refill your bottle of Hand Sanitizer in
* Kitchen * Automobile * Offices* Bathrooms *
125.11 FL OZ (3.7L)
* Please review the disclaimer below.
