Action Instant Hand Sanitizer
FDA Label NDC 80613-000

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Maestro Laboratories Sdn. Bhd. for the product Action Instant Hand Sanitizer (NDC 80613-000). 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 drug facts, active ingredient:, purpose, uses:, warnings:, when using this product, stop use and ask a doctor, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredient:

Alcohol Denat 75%

Purpose

Antimicrobial

Uses:

  • Hand sanitizer helps to reduce bacteria on the skin that could cause disease
  • Recommended for repeated use

Warnings:

FOR EXTERNAL USE ONLY

  • Flammable. Keep away from fire or flame.

When Using This Product

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

Stop Use And Ask A Doctor

if irritation or rash appears and lasts

Keep Out Of Reach Of Children.

  • If swallowed, get medical help or contact a Poison Control Center right away.

Direction Of Use:

Squeeze amount in your palm then briskly rub hands together until dry.

Children under 3 years of age should be supervised when using this product

Other Information:

Store below 110F (43C)

Inactive Ingredients:

Aqua, Glycerin, Acrylates/C10-30 Alkyl Acrylate Cross-polymer, Aminomethyl Propanol, Aloe Barbadensis Leaf Juice, Panthenol, Tocopheryl Acetate, Fragrance.

Questions Or Comments?

Call Customer Care Line 1300 88 4848

Package Labeling:

Bottle (Bottle)

Bottle (Bottle)

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