Active Ingredients
Ethyl Alcohol 70.0% v/v
Wellnicity Hand Sanitizer
FDA Label NDC 73009-017
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dibar Nutricional, S. De R.l. De C.v. for the product Wellnicity Hand Sanitizer (NDC 73009-017). 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 ingredients, purpose, warnings, do not use, keep out of reach of children., stop use and consult a doctor, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Anti Microbial
Warnings
Flammable: keep away from excessive heat or open flame.
For external use only.
Do Not Use
in or near eyes. In case of eye contact, flush with water. Do not apple to open wounds or damaged skin.
Keep Out Of Reach Of Children.
Stop Use And Consult A Doctor
if irritation occurs.
Directions
- Aplly entire packet to palm of hand. Use no water or towels. Rub until hands are completely covered.
Inactive Ingredients
Distilled Water, Biopol Plus / Carbomer 940, Aloe Vera Aqueous Extract, Aminomethyl Propane, Rapidgel.
Uses
- Hand sanitizer helps reduce bacteria on the skin could cause disease.
Package Labeling:
Box2 (Box2)
* Please review the disclaimer below.
