Active Ingredient:
Ethyl alcohol 70%
Meni Hand Sanitizer
FDA Label NDC 79439-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Seekr Global Inc. for the product Meni Hand Sanitizer (NDC 79439-000). 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:, inactive ingredients:, directions:, use:, warnings:, keep ouit of reach of children., do not use, stop use and consult a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredients:
Water, Propylene Glycol, Carbomer, Triethanolamine.
Directions:
Wet hands thoroughly with product and allow to dry without wiping, For children under 6, use only under adult supervision.
Use:
Health care personnel hand rub to help reduce bacteria that potentially can cause disease.
Warnings:
For external use only.
Flammable - keep away from fire or flames.
Keep Ouit Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center immediately.
Do Not Use
in eyes, In case of contact, rinse thoroughly with water.
Stop Use And Consult A Doctor If
irritation or redness develops and persist for more for more than 72 hours.
Package Labeling:125 Ml
Bottle (Bottle)
Package Labeling:500 Ml
Bottle2 (Bottle2)
Package Labeling:1000 Ml
Bottle3 (Bottle3)
* Please review the disclaimer below.
