Hand Sanitizer
FDA Label NDC 77357-000

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Desmoldantes Y Aditivos, S.a. De C.v. for the product Hand Sanitizer (NDC 77357-000). 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, purpose, uses, warnings, do not use, keep out of reach of children., directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol, 70% v/v

Purpose

Antimicrobial

Uses

  • Hand sanitizer, alcohol-based, used to kill bacteria in order to prevent diseases.
    • Ready to be used, as often as needed.

Warnings

For external use only
Flammable. Keep away from fire or flame

Do Not Use

near the eyes. In case of contact, rinse thoroughly with waterIf irritation develops, discontinue use and ask doctor.

Keep Out Of Reach Of Children.

If swallowed, get medical help or call a Poison Control Center immediately

Directions

  • Place a small amount in your hands and rub together until dry.
  • No rinsing required.

Inactive Ingredients

Glycerin, Polyacrylic acid.

Package Labeling: 33.81Oz/1L

Bottle (Bottle)

Bottle (Bottle)

Package Labeling: 1Gallon/3.785L

Bottle2 (Bottle2)

Bottle2 (Bottle2)

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