Active Ingredient
Alcohol 70% v/v
Hand Sanitizer
FDA Label NDC 74176-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by M3 Group Llc for the product Hand Sanitizer (NDC 74176-001). 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, use, warnings, do not use, when using this product, stop use and ask a doctor if, keep out of reach of children, 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 reduce bacteria on the skin. For use when soap and water are not available
Warnings
For external use only. Flammable. Keep away from fire or flame.
Do Not Use
■ in children less than 2 months of age ■ on open skin wounds
When Using This Product
■ avoid getting into the eyes. ■ in case of eye contact immediately flush eyes throughly with water
Stop Use And Ask A Doctor If
■ irritation or redness develops ■ conditions persist 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 ■ Supervise children under 6 years of age when using this product to avoid swallowing
Other Information
■ do not store above 105°F ■ may discolor fabrics or surfaces
Inactive Ingredients
water, glycerin, carbomer, aloe extract,sodium hydroxide
Package Label
Package Label (Sfhndsntzr250ml)
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