Hand Sanitizer
FDA Label NDC 79409-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Industrias Trevigo, S.a. De C.v. for the product Hand Sanitizer (NDC 79409-000). 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 drug facts, active ingredient:, purpose:, use:, warnings, when using this product, stop use and ask a doctor, 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
Active Ingredient:
Ethyl Alcohol 70%
Purpose:
Antimicrobial
Use:
Hand Sanitizer to help reduce bacteria on the skin.
Warnings
+ Flammable --- Keep away from fire or flame.
+ For external use only.
When Using This Product
+ do not use in or near the eyes. In case of contact, rinse eyes throughly with water.
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 product on hands.
+ Rub until dry.
Inactive Ingredients:
Water, Carbomer, Glycerin, T.E.A, Benzalkonium chloride, Fragrance ( Parfum ).
Other Information
+ Store below 110°C ( 43°F )
+ May discolor certain fabrics or surfaces.
Package Labeling: 236Ml
Label1 (Label1)
Package Labeling: 473Ml
Label2 (Label2)
Package Labeling: 1L
Label3 (Label3)
Package Labeling: 3.78L
Label4 (Label4)
Package Labeling: 1000L
Label5 (Label5)
* Please review the disclaimer below.
