Anti Bacterial Hand Sanitizer Gel
FDA Label NDC 78713-000

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Miworld Accesories Llc for the product Anti Bacterial Hand Sanitizer (NDC 78713-000). 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 ingredient, purpose, use, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Alcohol 75%

Purpose

Antiseptic

Use

For handwashing to decrease bacteria on the skin

Warnings

For external use only

Flammable, keep away from fire and flame

When Using This Product

  • Avoid the eyes and mucous membranes
  • In the case of eyes or mucous membranes contact, rinse area thoroughly with water

Stop Use And Ask A Doctor If

  • Condition worsens
  • Redness or irritation develop
  • Condition persists for more than 3 days

Keep Out Of Reach Of Children.

If swallowed, contact a doctor or Poison Control Center immediately

Directions

Wet hands thoroughly with product and allow to dry without wiping.

Other Information

  • Store Below 105 °F
  • May discolor some fabrics

Inactive Ingredients

Water, Carbomer, Aminomethyl Propanol.

Package Labeling:60Ml

Label (Label)

Label (Label)

Package Labeling:236Ml

Label2 (Label2)

Label2 (Label2)

* Please review the disclaimer below.