Myterra Hand Sanitizer Foam Na Soap
FDA Label NDC 70780-151

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Portionpac Chemical Corporation for the product Myterra Hand Sanitizer Foam Na (NDC 70780-151). 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, ​uses​, ​warnings, otc - keep out of reach of children, ​directions, ​inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

​Active Ingredient

Benzalkonium Chloride 0.1%

​Purpose

Antimicrobial

​Uses​

  • For hand sanitizing to decrease bacteria on the skin
  • Recommended for repeated use

​Warnings

​For external use only​.

​When using this product​ avoid contact with eyes.  In case of eye contact, flush eyes with water.

​Stop use and ask a doctor if​ irritation or redness develops, or if condition persists for more than 72 hours.

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.

​Directions

  • Pump a small amount of foam into palm of hand.
  • Rub thoroughly over all surfaces of both hands.
  • Rub hands together briskly until dry.

​Inactive Ingredients

Water, cetrimonium chloride, laurtrimonium chloride, dihydroxyethyl cocamine oxide, glycereth-17 cocoate, citric acid, fragrance

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