D7 DECON SEVEN- n/a liquid

D7 Decon Seven by

Drug Labeling and Warnings

D7 Decon Seven by is a Otc medication manufactured, distributed, or labeled by Morgan Gallacher Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride.........0.1 %

Uses

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

Purpose

Antimicrobial

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

• 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

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

D7 Foaming Hand Sanitizer

Kills up to 99.9999% of Germs Cleans and Protects

D7 Foaming Hand Sanitizer is based on the active ingredient Bezalkonium Chloride in a unique, non-drying, moisturizing and conditioning formulation.  D7 Foaming Hand Sanitizer kills >99.9% of most common germs that may cause illness in just 15 seconds. 

In comparison to alcohol-based hand sanitizers, D7 Foaming Hand Sanitizer is non-fammable, non-staining and less drying to skin.  Published studies report that Benzalkonium Chloride hand sanitizers, like D7 Foaming Hand Sanitizer, demonstrated greater sustained degerming activity than gelled alcohol hand sanitizers.  Alcohol-based hand sanitizers were found to become less effective with repeated use.  

50 ml

550 ml

1 Gallon

INGREDIENTS AND APPEARANCE

D7 DECON SEVEN 
n/a liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50241-028
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50241-028-00	49.62 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/09/2020
2	NDC: 50241-028-06	545.82 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/09/2020
3	NDC: 50241-028-04	3756.64 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/09/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/09/2020

Labeler - Morgan Gallacher Inc. (028311595)

Registrant - Morgan Gallacher Inc. (028311595)

Establishment
Name	Address	ID/FEI	Business Operations
Morgan Gallacher Inc.		028311595	manufacture(50241-028) , api manufacture(50241-028) , pack(50241-028)