Uncle Jeds Cold Remedy Hand Sanitizer
FDA Label NDC 81172-000

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Earth Sense Energy Systems, Inc for the product Uncle Jeds Cold Remedy Hand Sanitizer (NDC 81172-000). 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, uses:, warnings:, 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.

Drug Facts

Active Ingredient

Ethyl Alcohol (Ethanol) 75%

Purpose

Antiseptic

Uses:

Helps reduce bacteria on the skin that could cause disease. Recommended for repeat use.

Warnings:

For external use ONLY. Flammable. Keep away from fire or flame.

When Using This Product:

Do not use in or near the eyes. In case of eye contact, flush eyes thoroughly with water.

Stop Use And Ask A Doctor If:

Irritation and redness develops and lasts more than 72 hours.

Keep Out Of Reach Of Children:

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Place enough product into palm to thoroughly cover your hands. Rub hands together briskly until dry. Children under 6 years of age should be
supervised when using this product. Not recommended for infants. Other information: Store below 110°F (43°C). May discolor certain fabrics or
surfaces.

Inactive Ingredients:

Water, Aloe Barbadensis Leaf Extract, Acrylates/C10-30 alkyl Acrylate Crosspolymer, Tetrahydroxypropyl Ethylenediamine, Vitamin E, Peppermint Scent.

Package Labeling

500 mL (Label)

500 mL (Label)

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