Otc - Active Ingredient
ALCOHOL 80% V/V. PURPOSE: ANTISEPTIC
Hand Sanitizer
FDA Label NDC 74105-900
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Deviation Distilling Llc for the product Hand Sanitizer (NDC 74105-900). 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 otc - active ingredient, otc - purpose, dosage & administration, warnings, inactive ingredient, indications & usage, otc - keep out of reach of children, 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
Otc - Purpose
ANTISEPTIC
Dosage & Administration
Directions: Place enough product on hands to cover all surfaces. Rub hands together until dry.
Warnings
Warnings: For external use only. Flammable. Kepp away from heat or flame.
Inactive Ingredient
Inactive Ingredients: glycerin, hydrogen peroxide, purified water USP
Indications & Usage
Use(s): Hand santitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children: If swallowed, get medical help or contact a Poison Control Center right away.
Package Label.Principal Display Panel
3785mL 74105-900-01
Hand Sanitizer Gallon.jpg
236.59 mL 74105-900-08
SIZE: 88.72 mL
NDC: 74105-900-03
IMAGE: 3oz bottle label.jpg
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