Antimicrobial Hand Sanitizer
FDA Label NDC 76939-555

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Nvip Llc for the product Antimicrobial Hand Sanitizer (NDC 76939-555). 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, 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 Ingredient

Alcohol 70% v/v

Purpose

Antimicrobial

Use[S]

Hand sanitizer to help reduce bacteria on the skin that could cause disease. Recommended for repeated use.

Warnings

Flammable. Keep away from fire or flame.

For External use only.

Do Not Use

  • on children less than 2 months of age
  • on open skin wounds

When Using This Product

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop Use And Ask A Doctor

if irritation or rash appears and lasts.

Keep Out Of Reach Of Children.

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

Directions

  • Place enough product in your palm to thoroughly cover your hands.
  • Rub hands together briskly together until dry.
  • Children under 6 years of age should be supervised when using this product.

Inactive Ingredients

Water (Aqua), Isopropyl Alcohol, PEG-12 Dimethicone, Caprylyl Glycol, Glycerin, Isopropyl Myristate, Tocopheryl Acetate.

Other Information

  • Store between 54-84°F (15-30°C)
  • May discolor certain fabrics or surfaces

80182-001-12

Bottle (Bottle)

Bottle (Bottle)

80182-001-16

Bottle2 (Bottle2)

Bottle2 (Bottle2)

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