MyTerra Hand Sanitizer Foam NA: Package Insert and Label Information

MYTERRA HAND SANITIZER FOAM NA- benzalkonium chloride soap
PortionPac Chemical Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

​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.

​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

Case Label -- 8 x 1000 mL
(click image for full-size original)

MYTERRA HAND SANITIZER FOAM NA
benzalkonium chloride soap
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:70780-151
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 1.00 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER
CETRIMONIUM CHLORIDE
LAURTRIMONIUM CHLORIDE
DIHYDROXYETHYL COCAMINE OXIDE
GLYCERETH-17 COCOATE
CITRIC ACID MONOHYDRATE
Product Characteristics
Color white (water white — colorless, dispensed as a white foam) Score
Shape Size
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70780-151-13 8 BAG in 1 BOX contains a BAG
1 1000 mL in 1 BAG This package is contained within the BOX (70780-151-13)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 10/30/2017
Labeler — PortionPac Chemical Corporation (005448584)

Revised: 12/2022 PortionPac Chemical Corporation

DrugInserts.com provides trustworthy package insert and label information about marketed drugs as submitted by manufacturers to the US Food and Drug Administration. Package information is not reviewed or updated separately by DrugInserts.com. Every individual package label entry contains a unique identifier which can be used to secure further details directly from the US National Institutes of Health and/or the FDA.

As the leading independent provider of trustworthy medication information, we source our database directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. Our material is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2023. All Rights Reserved.