Hand Sanitizer Gel
FDA Label NDC 73288-008

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Tianbo First Aid Product Co., Ltd. for the product Hand Sanitizer (NDC 73288-008). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - keep out of reach of children, dosage & administration, storage and handling, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Active ingredient

Alcohol 62% v/v

Otc - Purpose

Purpose  Antiseptic

Indications & Usage

Uses

For hand sanitizing to decrease bacteria on skin without soap and water

Warnings

Warnings

For external use only.

Flammable: keep away from heat or flame

Do not use in the eyes

Use with caution if allergic to alcohol

Otc - Keep Out Of Reach Of Children

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

Dosage & Administration

Directions:

Put enough product on your palm to cover hands and briskly rub hands until dry
Wet hands thoroughly with product and allow to dry without wiping

  • For children under 6, use only under adult supervision.

Storage And Handling

Other information

  • Do not store above 105 F
  • May discolor some fabrics
  • Harmful to wood finishes and plastics

Inactive Ingredient

Inactive ingredients

Acrylates/C10-30Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Aloe Barbadensis Leaf Juice, Denatonium Benzoate, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate, Water (Aqua).

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