Hand Sanitizer
FDA Label NDC 51774-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Industrias Chamer Sa De Cv for the product Hand Sanitizer (NDC 51774-001). 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 other, active ingredient, purpose, directions, warnings, otc - keep out of reach of children, otc - stop use, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Other

Drug Facts

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Directions

Massage onto hands. Apply at least twice daily or as often desired. Avoid contact with eyes. Not for consumption.

Warnings

For external use only. Flammable — Keep away from fire or flame

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children if swallowed, get medical help or contact a Poison Control Center right away.

Otc - Stop Use

  • Stop use and ask a doctor if irritation or redness develop and lasts more than 72 hours.

Other Information

  • Do not store above 105 °F (40 °C).
  • May discolor certain wood surfaces.

Inactive Ingredients

Water (Aqua), Glycerin, Carbomer, Aloe Barbadensis Extract, Triethanolamine, Methylisothiazolinone (and) Iodopropynil Butil Carbamate.

Questions?

Call +1 (786) 785-8074
www.grupochamer.com

Principal Display Panel - 1,000 Ml Bottle

Puriderm™

HAND SANITIZER
ANTIBACTERIAL
70% ETHYL ALCOHOL

KILLS 99.99% OF GERMS

APPROVED
FDA
REGISTERED

WITH ALOE VERA AND GLYCERIN
SOFT ON THE SKIN

℮ 34 FL OZ (1,000 mL)

Principal Display Panel (1,000 mL Bottle)

Principal Display Panel (1,000 mL Bottle)

* Please review the disclaimer below.