Advanced Hand Sanitizer With Aloe Bottles
FDA Label NDC 77650-080

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by North Park Enterprises, Lc for the product Advanced Hand Sanitizer With Aloe Bottles (NDC 77650-080). 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, uses., warnings, stop use and ask a doctor, keep out of reach of children., directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Drug Facts

Active Ingredient

Ethyl Alcohol 80%

Uses.

Helps reduce bacteria on the skin that can cause sickness, recommended for repeated use.

Warnings

For external use only 

  • Avoid contact with eyes.If contact occurs, flush with water.

Stop Use And Ask A Doctor

if, in rare instances, redness or irritation develops and persists for over 72 hours

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a poison control center.

Directions

Apply a small amount to palms, rubbing briskly to cover both hands until dry-repeat as necessary.

Inactive Ingredients

Water, Aloe Barbadensis Leaf Powder, Glycerin, Hydroxypropylcellulose, Hydrogen Peroxide.

Package Labeling

Label (Label)

Label (Label)

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