Hand Sanitizer Gel
FDA Label NDC 77129-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Travel Retail Global Inc. for the product Hand Sanitizer (NDC 77129-001). 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 ingredient, purpose, use, warnings, when using this product, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredient

Alcohol 75%

Purpose

Antiseptic

Use

  • For handwashing 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 serious gastric disturbances will result.

When Using This Product

  • Avoid the eyes and mucous membrances
  • In the case of eyes or mucous membranes contact, rinse area thoroughly with water
  • In case of deep or puncture wounds or serious burns, consult physician.
  • If redness, irritation, swelling, or pain persists or increases or if infection occurs discontinue use and consult physician.

Keep Out Of Reach Of Children.

  • If swallowed,contact a doctor or Poison Control Center immediately.

Directions

  • Rub drime 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, Aloe Barbadensis Leaf Juice, Carbomer, Triethanolamine.

Package Labeling:

Bottle (Bottle)

Bottle (Bottle)

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