Shoff Hand Sanitizer
FDA Label NDC 78021-370

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Himmelgeister Inc. Dba Hba Global for the product Shoff Hand Sanitizer (NDC 78021-370). 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 ingredients, purpose, uses, inactive ingredients:, directions:, warnings:, 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 Ingredients

Ethyl Alcohol 70% V/V

Purpose

Antiseptic

Uses

  • hand sanitizer to decrease bacteria on the skin

Inactive Ingredients:

Water, Glycerin, Propylene Glycol, Carbomer, Triethanolamine, Aloe Barbadensis Leaf Extract, PARFUM, Tocopheryl Acetate(Vitamin E)

Directions:

  • Wet your hands thoroughly with the SHOFF Hand Sanitizer, rub until dry without wiping.
  • For children under6, use ONLY under adult supervision.
  • Not recommended for infants.

Warnings:

  • For external use only: hands
  • Flammable, keep away from fire or flame
  • Keep out of reach of children
  • Do not store above 100F(38C)
  • May discolor fabrics
  • Harmful to wood finishes and plastics

    • When using this product:

    • Keep out of eyes
    • In Case of contact of eyes, flush thoroughly with water
    • Avoid contact with broken skin
    • Do not inhale or ingest

Keep Out Of Reach Of Children

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

Packaging

Image (Final)

Image (Final)

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