Instant Hand Sanitizer
FDA Label NDC 79699-000

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Zidac Laboratories Ltd for the product Instant Hand Sanitizer (NDC 79699-000). 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, when using this product, stop use and ask a doctor, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol 77%v/v

Purpose

Antimicrobial

Uses

  • Hand sanitizer helps reduce bacteria on the skin
  • Recommended for repeated use

Warnings

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

When Using This Product

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

Stop Use And Ask A Doctor

if irritation or rash occurs and lasts.

Keep Out Of Reach Of Children.

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

Directions

  • Place product in palm of hand 
  • Rub hands together until dry
  • Supervise children under 6 years of age when using product

Storage

Store below 110°F (43°C)

Inactive Ingredients

Water (Aqua), Glycerin, Carbomer, Aminomethyl Propanol, Fragrance (Parfum), Aloe Barbadensis Leaf Juice, Propylene Glycol

Package Labeling: 100Ml

Bottle (Bottle)

Bottle (Bottle)

Package Labeling: 500Ml

Bottle2 (Bottle2)

Bottle2 (Bottle2)

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