Hand Sanitizer Gel
FDA Label NDC 74640-010

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Gordon Industries for the product Hand Sanitizer (NDC 74640-010). 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 active ingredient, purpose, use, warnings, does not, when using this product, 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

Active Ingredient

Alcohol 75%

Purpose

Antiseptic

Use

For hanwashing to decrease bacteria on the skin

Warnings

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

Does Not

contain grain alcohol; do not drink. if taken internally will produce serious gastric disturbance.

When Using This Product

  • Avoid the eyes and mucous membranes
  • In the case of eyes or mucous membranes contact, rinse area thoroughly with water

Stop Use And Ask A Doctor If

  • Condition worsens
  • Redness or irritation develops
  • Condition persists for more than 3 days

Keep Out Of Reach Of Children

If swallowed, contact a doctor or Poison Contorl Center immediately.

Directions

  • Rub dime sized amount between hands until dry.
  • Supervise children in the use of this product.
  • In the case of eye contact, rinse eyes thoroughly with water.

Other Information

  • Store below 105 °F
  • May discolor some fabrics.

Inactive Ingredients

Water,Glycerin, Propylene Glycol, Carbomer, Aminomethyl Propanol.

Questions?

516-354-8888

Package Labeling: (74640-010-30)

Label (Label)

Label (Label)

Package Labeling: (74640-010-50)

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