Active Ingredient
ethyl alcohol % 70 V/V
Dr.phi Advanced Hand Sanitizer
FDA Label NDC 58161-156
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 Advanced Hand Sanitizer (NDC 58161-156). 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, indications & usage, warning, keep out of reach of children, when using this product, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
antimicrobial
Uses
hand sanitizer to help reduce bacteria on the skin that could cause disease
Indications & Usage
hand sanitizer to help reduce bacteria on the skin that could cause disease
Warning
flamable , keep away from fire or flame
for external use only
Keep Out Of Reach Of Children
if swallowed get medical help or contact a poison control centre right away
When Using This Product
do not use in or near the eyes , in case of contact rinse eyes thoroughly with water
Stop Use And Ask A Doctor If
irritation and rash appears and lasts
Directions
place enough prduct on your palm to thoroughly cover your hands
rub hands together until dry
Other Information
store below 110° F
may discolor certian fabrics or surfaces
Inactive Ingredients
water , glycerin , carbomer , PEG-40 hydrogentated castor oil , aminomethyl propanol, fragrance , EDTA disodium, BHT, tocopheryl acetate , aloe barbadensis (aloe vera) leaf extract.
Package Label.Principal Display Panel
Label (Label)
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