E3 FOAMING HAND SANITIZER- n/a liquid

E3 Foaming Hand Sanitizer by

Drug Labeling and Warnings

E3 Foaming Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Morgan Gallacher Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Active Ingredient

Benzalkonium Chloride .......0.1 %

Uses

Uses

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

Purpose

Purpose

Antimicrobial

Warnings

Warnings

• For external use only
• When using this product avoid contact with eyes. In case of eye contact, flush eyes with water. Do not ingest.
• Stop use and ask a doctor if irritation or redness develops and conditions persist.

Keep out of reach of children.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Conrol Center right away.

Directions

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

Inert Ingredients:

Inactive Ingredients

• water
• cetrimonium chloride
• laurtrimonium chloride
• dihydroxyethyl cocamine oxide
• glycereth-17 cocoate
• citric acid

E3 Foaming Hand Sanitizer

E3 Foaming Hand Sanitizer

INGREDIENTS AND APPEARANCE

E3 FOAMING HAND SANITIZER 
n/a liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50241-986
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	.10 g  in 100 g

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	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50241-986-02	4 in 1 PACKAGE	09/23/2018
1	NDC: 50241-986-01	3756 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		09/23/2018

Labeler - Morgan Gallacher Inc. (028311595)

Registrant - Morgan Gallacher Inc. (028311595)