Active Ingredient
Ethyl Alcohol 70% V/V
Dr.phi Instant Hand Sanitizer
FDA Label NDC 58161-155
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Mamiba for the product Dr.phi Instant Hand Sanitizer (NDC 58161-155). 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, drug facts, purpose, uses, warnings, 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
Drug Facts
Label 10 mL (51945 4)
Purpose
Antimicrobial
Uses
HAND SANITIZER TO HELP REDUCE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE
HAND SANITIZER TO HELP REDUCE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE
Warnings
Flammable, keep away from fire or flame.
For external use only
Stop Use And Ask A Doctor
if irritation or rash appears and lasts
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 until dry Children under 6 years of age should be supervised when using this product
Other Information
Store below 110°F (43°C)
May discolor certain fabrics or surfaces
Inactive Ingredients
Water (aqua), glycerin, Carbomer, Aminmethylpropanol
* Please review the disclaimer below.
