Active Ingredient
Ethyl Alcohol 70% v/v
Medichoice Instant Hand Sanitizer Gel
FDA Label NDC 39892-0400
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by O&m Halyard, Inc. for the product Medichoice Instant Hand Sanitizer (NDC 39892-0400). 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, do not use, 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
Uses
- hand sanitizer to help reduce bacteria on the skin
Warnings
Flammable. Keep away from fire or flame
For external use only - hands.
Do Not Use
in or near the eyes. In case of contact, rinse eyes thoroughly with water
Stop Use And Ask A Doctor
if skin irritation and redness or rash develops.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- place enough product in your palm to thoroughly cover your hands
- rub hands together briskly until dry
- children under 6 years of age should be supervised when using this product
- not recommended for infants
Other Information
- store at normal room temperature
- may discolor certain fabrics
- may be harmful to wood finishes and plastics
Inactive Ingredients
Purified Water, Isopropyl Alcohol, Propylene Glycol, Fragrance, Aloe Barbadensis Leaf Juice (Decolorized), Carbomer, Glycerin, Aminomethyl Propanol, Isopropyl Myristate, Tocopheryl Acetate
Package Labeling: (39892-0400-1)
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