Hand Sanitizer Gel
FDA Label NDC 22431-585

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Blue Cross Laboratories, Inc. for the product Hand Sanitizer Gel (NDC 22431-585). 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, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, storage and handling, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Active ingredients purpose

Ethyl Alcohol 70% Antiseptic

Otc - Purpose

Uses

  • to decrease bacteria on the skin that could cause disease
  • recommended for repeated use

Package Label.Principal Display Panel

Hand Rx

Hand Sanitizer Gel

70% Alcohol

Advanced formula Clean Scent

Net Contents: 1 Gallon (3.78L)

Hand Rx

Hand Sanitizer Gel

70% Alcohol

Advanced formula Clean Scent

Net Contents: 1 Gallon (3.78 L)

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