OTC Medication Information: Safeguard Hand Sanitizer

SAFEGUARD HAND SANITIZER- alcohol gel
The Procter & Gamble Manufacturing Company

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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

When using this product

  • Do not use in or near eyes
  • Use in a well-ventilated area
  • Discontinue use if irritation and redness develop

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

Sfg
(click image for full-size original)
SAFEGUARD HAND SANITIZER
alcohol gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:37000-603
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 64 g in 100 mL
Inactive Ingredients
Ingredient Name Strength
TROLAMINE
GLYCERIN
GLYCERETH-2 COCOATE
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:37000-603-40 1200 mL in 1 BAG None
2 NDC:37000-603-53 532 mL in 1 BOTTLE, PUMP None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 07/01/2010
Labeler — The Procter & Gamble Manufacturing Company (004238200)

Revised: 08/2023 The Procter & Gamble Manufacturing Company

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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