Active Ingredient
Alcohol 62%
Hand Sanitizer
FDA Label NDC 74175-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Elevate Skincare, Inc. for the product Hand Sanitizer (NDC 74175-001). 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
■ hand sanitizer to help reduce bacteria on the skin
Warnings
Flammable. Keep away from fire or flame. For external use only
When Using This Product
■ avoid getting into the eyes. ■ In case of eye contact immediately flush eyes thoroughly with water
Stop Use And Ask A Doctor If
■ if irritation or redness develops ■ condition persists for more than 72 hours ■ redness is present
Keep Out Of Reach Of Children
In case of accidental ingestion, contact a doctor or Poison Control Center immediately.
Directions
■ place enough product in your palm to thoroughly cover both hands ■ rub hands together until dry ■ no rinsing required
Other Information
■ do not store above 105°F ■ may discolor some fabrics or surfaces
Inactive Ingredients
carbomer, deionized water, propylene glycol, sodium hydroxide
Package Label
Package Label (Hndsntzrelvte)
* Please review the disclaimer below.
