Dosage & Administration
Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Hand Sanitizer
FDA Label NDC 78763-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Lubdeco S.a. De C.v. for the product Hand Sanitizer (NDC 78763-101). 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 dosage & administration, otc - active ingredient, inactive ingredient, indications & usage, otc - keep out of reach of children, otc - purpose, warnings, 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 - Active Ingredient
Alcohol 70% v/v. Purpose: Antiseptic
Inactive Ingredient
Carbomer
Triethanolamine
Glycerin
Purified Water
Indications & Usage
Place enough product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age using this product to avoid swallowing.
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.
Otc - Purpose
Antiseptic
Warnings
For external use only. Flammable. Keep away from fire or flame
Package Label.Principal Display Panel
1L NDC: 78763-101-01
3.78L NDC: 78763-101-04
2.5ml NDC: 78763-101-99
* Please review the disclaimer below.
