Instant Hand Sanitizer
FDA Label NDC 80575-003

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by National Design Llc for the product Instant Hand Sanitizer (NDC 80575-003). 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 ingredient:, purpose:, uses:, warnings:, when using this product:, directions:, ingreidients:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Drug Facts

Active Ingredient:

Ethyl Alcohol 68%

Purpose:

Antiseptic

Uses:

  • Hand sanitizer reduce bacteria on skin

Warnings:

Flammable, Keep away from fire and flame.

For external use only

When Using This Product:

do not use in or near eyes, in case of contact, rinse eyes thoroughly with water.

Directions:

Place product on hands, rub untill dry

Ingreidients:

Glycerin, propylene glycol, triethanolamine, carbomer, fragrance, disodium edta,tocopheryl acetate, deionized water.

Package Labeling:

Bottle7 (Bottle7)

Bottle7 (Bottle7)

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