Active Ingredient
Ethyl Alcohol 75% v/v
Covidizer Hand Sanitizer
FDA Label NDC 78715-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Covidizer, Llc for the product Covidizer Hand Sanitizer (NDC 78715-000). 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, purpose, uses, warnings, do not use, when using this product,, stop use and ask a doctor if, keep out of reach of children., 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 decrease bacteria on the skin, when water, soap & towel are not availble.
- recommended for repeated use.
Warnings
For external use only. Flammable. Keep away from fire or flame.
Do not apply around eyes.
Do Not Use
in ears & mouth.
When Using This Product,
avoid contact with eyes. In case of contact flush eyes with water.
Stop Use And Ask A Doctor If
redness or irritation develop and persist for more than 72 hours.
Keep Out Of Reach Of Children.
Children must be supervised in use of this product.
Directions
- pump as needed into your palms and thoroughly spread on both hands.
- rub into skin until dry.
Other Information
- store at 20°C (68°F to 77°F).
- may discolor fabrics.
Inactive Ingredients
Water, PEG-40 Hydrogenated Castor Oil, Chloroxylenol, Carbomer, Trolamine.
Package Labeling:30Ml
Label (Label)
Package Labeling:60Ml
Label2 (Label2)
Package Labeling:237Ml
Label3 (Label3)
Package Labeling:1000Ml
Label4 (Label4)
Package Labeling:2000Ml
Label5 (Label5)
* Please review the disclaimer below.
