Safeguard Gel
FDA Label NDC 37000-603

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by The Procter & Gamble Manufacturing Company for the product Safeguard (NDC 37000-603). 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, uses, 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

Ethanol 64%

Purpose

Hand Sanitizer

Uses

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

Warnings

  • For external use only
  • Flammable, keep away from fire or flame

Otc - When Using

When using this product

  • Do not use in or near eyes
  • Use in a well-ventilated area

Otc - Stop Use

  • Discontinue use if irritation and redness develop

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

Directions

  • Receive a small amount of liquid into palm of hand
  • Rub thoroughly over all surfaces of both hands
  • Rub hands together until dry

Other Information

  • Store in a cool dry place below 104° F

Inactive Ingredients

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, glycereth-2-cocoate, glycerine, triethanolamine, water

Questions?

Contact Procter & Gamble Professional® Mon-Fri 9am - 5pm EST at 1-800-332-7787

Principal Display Panel - 1.2L Bag Label

Procter & Gamble
Professional®

Safeguard®

Hand Sanitizer Gel
Alcohol Hand Sanitizer Gel

1.2L (1.26 QT) 40.5 FL OZ

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