Hand Sanitizer
FDA Label NDC 67510-0487

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Kareway Product, Inc. for the product Hand Sanitizer (NDC 67510-0487). 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, keep out of reach of children, uses, warnings, when using this product, stop use and ask a doctor if, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol  62%    

Purpose

Antiseptic

Keep Out Of Reach Of Children

In case of a accidental ingestion, seek professional assistance or contact a Poison control Center immediately.

Uses

  • To decrease bacteria on the skin.
  • Recommended for repeated use.

Warnings

For external use only-hands.
Flammable. Keep away from hear or flame.

When Using This Product

  • Keep out of eyes. In case of contact with eyes, flush throughly with water.
  • Avoid contact with broken skin.

Stop Use And Ask A Doctor If

skin irritation developes

Directions

  • Wet hands throughly with product and allow to dry without wiping.
  • For children under 6, use only under adult supervision
  • Not recommended for infants.

Other Information

  • Store at 20° to 25°C (68° to 77°F)

Inactive Ingredients

Water, Glycerin, Propylene Glycol, Carbomer, Fragrance, Isopropyl Alcohol, Sodium Hydroxide, Isopropyl Myristate, Tocopheryl Acetate, Aloe Vera Extract

Package Label.Principal Display Panel

Image Of Bottle Label (Handsanitizergel)

Image Of Bottle Label (Handsanitizergel)

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