Premium Hand Sanitizer
FDA Label NDC 69898-801

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Md Science Lab Llc for the product Premium Hand Sanitizer (NDC 69898-801). 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 other, active ingredient, purpose, use, warnings, otc - when using, otc - stop use, otc - 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

Other

Drug Facts

Active Ingredient

Ethyl Alcohol 80%

Purpose

Antimicrobial

Use

  • For hand sanitizing to decrease bacteria on the skin
  • Recommended for repeated use

Warnings

  • For external use only.

Otc - When Using

  • When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

Otc - Stop Use

  • Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Dispense a small amount into palm of hand.
  • Rub thoroughly over all surfaces of both hands.
  • Rub hands together briskly until dry.

Inactive Ingredients

Deionized Water, Glycerin, Hydrogen Peroxide.

Principal Display Panel - 3.7 Liter Bottle Label

M.D.
Science Lab
LLC

PREMIUM
hand
sanitizer

Kills 99.99% of Germs

moisturizes & softens skin

1 gal 128 fl oz 3.7 liter e

Principal Display Panel (3.7 liter Bottle Label)

Principal Display Panel (3.7 liter Bottle Label)

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