Genuine First Aid Hand Sanitizer Cream
FDA Label NDC 50814-078

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Gfa Production(xiamen) Co.,ltd for the product Genuine First Aid Hand Sanitizer (NDC 50814-078). 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, do not use, stop use and ask a doctor if, 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

Ethyl Alcohol 62% v/v

Purpose

Antiseptic

Uses

  • For handwashing to decrease bacteria on the skin 
  • Recommended for repeated use.

Warnings

Flammable, keep away from fire or flame

For external use only.

Do Not Use

  • in the eyes.

Stop Use And Ask A Doctor If

  • irritation and redness develop
  • condition persists for more than 72 hours

Keep Out Of Reach Of Children.

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

Directions

  • Wet hands thoroughly with product and allow to dry without wiping.

Other Information

Store at 15° to 25°C (59° to 77°F)

Inactive Ingredients

Acrylates/C 10-30 alkyl acrylate crosspolymer, Aloe Barbadensis Leaf Juice, Fragrance, Glycerin, Maltodextrin, Propylene Glycol, Triethanoamine, Tocopheryl Acetate, Water

Package Labeling:

Label03 (Label03)

Label03 (Label03)

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