Vegol Hand Sani
FDA Label NDC 78244-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Grupo Asavalle, S.a. De C.v. for the product Vegol Hand Sani (NDC 78244-001). 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 ingredients, purpose, uses, 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 Ingredients
Ethyl Alcohol 70%
Purpose
Antiseptic
Uses
To decrease bacteria on hands.
Warnings:
Flammable: Keep away from flame or high heat.
For external use only.
When Using This Product
keep out of eyes,
Stop Use, And Ask A Doctor
if irritation or redness develops.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions:
Wet hands thoroughly with product and allow to dry without wiping.
Other Information:
Do not store above 105°F. May discolor some fabrics. Harmful to wood finishes and plastics.
Inactive Ingredients:
Water, Glycerin, Carbomer, Triethanolamine, polysorbate, Fragrance (Parfume).
Package Labeling: 1L
Label1 (Label1)
Package Labeling: 4L
Label2 (Label2)
* Please review the disclaimer below.
