MYTERRA HAND SANITIZER FOAM NA- benzalkonium chloride soap

MyTerra Hand Sanitizer Foam NA by

Drug Labeling and Warnings

MyTerra Hand Sanitizer Foam NA by is a Otc medication manufactured, distributed, or labeled by PortionPac Chemical Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

​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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

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

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.00 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)
GLYCERETH-17 COCOATE (UNII: 3057VPT0KC)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Product Characteristics
Color	white (water white - colorless, dispensed as a white foam)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70780-151-13	8 in 1 BOX	10/30/2017
1		1000 mL in 1 BAG; Type 0: Not a Combination Product

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)