Hands Hand Sanitizer
FDA Label NDC 79792-000

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Camstar Paper Inc. for the product Hands Hand Sanitizer (NDC 79792-000). 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 active ingredients, purpose, use(s), warnings, do not use, when using this product, stop use and ask a doctor, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

Ethyl alcohol 75 % v/v

Purpose

Antimicrobial

Use(S)

Hands Hand Sanitizer to help reduce bacteria that potential can cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame.

Do Not Use

  • in children less than 2 months of age.
  • On open skin wounds.

When Using This Product

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop Use And Ask A Doctor

if irritation or rash occurs. These may be signs of a serious condition.

Keep Out Of Reach Of Children.

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

Directions

Place enough product on hands to cover all surfaces. Rub hands together until dry.

Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

  • Store between 15-30°C(59-86°F).
  • Avoid freezing and excessive heat about 40°C (104°F)

Inactive Ingredients

glycerin, hydrogen peroxide, purified water USP, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propane, Phenoxyethanol, fragrance.

Package Labeling:500Ml

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Label (Label)

Package Labeling:250Ml

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