Active Ingredient(S)
Ethyl Alcohol 75% v/v. Purpose: Antiseptic
Instant Hand Sanitizer
FDA Label NDC 75819-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Naftali Inc for the product Instant Hand Sanitizer (NDC 75819-001). 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 active ingredient(s), purpose, uses, warnings, keep out of reach of children, directions, inactive ingredients, package label - principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic, Hand Sanitizer
Uses
For hand sanitizing to decrease bacteria on skin.
Warnings
Flammable. Keep away fire or flame.
For external use only. Keep out of eyes. If eye contact occured, flush immediately with water and call a doctor. Stop use and ask a doctor if irritation develops.
Keep Out Of Reach Of Children
Call a doctor or Poison Center if swallowed.
Directions
Apply a pea sized amount onto your hand, and rub throughly until dry.
Use as needed. For children under 6, use with adult supervision.
Inactive Ingredients
glycerin, hydrogen peroxide, purified water USP
Package Label - Principal Display Panel
500 mL NDC: 75819-001-01
500ml Label (500)
* Please review the disclaimer below.
