Antisepctic Hand Sanitizer 100
FDA Label NDC 75292-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Jg Atlas Comercios, S.a. De C.v. for the product Antisepctic Hand Sanitizer 100 (NDC 75292-001). 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, do not use, stop using 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.

Active Ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Use

for hand washing to decrease bacteria on the skin

Warnings

For external use only.
Flammable, keep away from fire or flame.

Do Not Use

in the eyes

Stop Using And Ask A Doctor If

  • irritation and redness develop
  • condition persists for more than 72 hours

Keep Out Of Reach Of Children

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

Directions

wet hands thoroughly with product and allow to dry without wiping

Other Information

  • store in a cool and dry place
  • do not refill container in a closed space as vapors may be flammable.

Inactive Ingredients

camphor, carbomer, glycerin, menthol, methylchlorothiazolinone, methylisothiazolinone, mint extract, triethanolamine, water

​Package Labeling:

Label (Label)

Label (Label)

* Please review the disclaimer below.