Active Ingredient
Ethyl Alcohol 70% v/v
Hand Sanitizer
FDA Label NDC 74341-194
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Newacme Llc for the product Hand Sanitizer (NDC 74341-194). 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, 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 hand washing to decrease bacteria ont he skin.
Warnings
Flammable. Keep away from fire or flame.
For External Use Only
When Using This Product
avoid contact with eyes. If contact occurs rinse eyes thoroughly with water.
Stop Use And Ask A Doctor
if skin irritation or rash develops and continues for more than 72 hours.
Keep Out Of Reach Of Children.
If swallowed get medical help or contact your Poison Control right away.
Directions
- Place a palmful (5 grams) of product in one hand.
- Spread on both hands and rub into skin until dry (approximately 1 to 2 minutes).
Other Information
- Do not store above 105°F,
- May discolor some fabrics.
- Harmful to wood finishes and plastics.
Inactive Ingredients
Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate, Triethanolamine, Water
Package Labeling: 15 Ml
Label (Label)
Package Labeling: 53 Ml
Label2 (Label2)
Package Labeling: 60 Ml
Label3 (Label3)
Package Labeling: 473 Ml
Label4 (Label4)
* Please review the disclaimer below.
