MG FOAMSAN- benzalkonium chloride liquid

MG FoamSan by

Drug Labeling and Warnings

MG FoamSan by is a Otc medication manufactured, distributed, or labeled by Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.. 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, if condition persists for more than 72 hours. 

Keep out of reach of children.

Keep out of reach of children. If swallowed, get medical help

or contact a Poison Control Center immediately.

Directions

-Pump a small amount of foam into palm of hand.  

-Rub thoroughly over all surfaces of both hands.  

-Rub hands together brisky until dry

Inactive Ingredients

Water, Cocamidopropyl PG-dimonium Chloride Phosphate, Dihydroxyethyl cocamine oxide, acetamidoethoxyethanol, citric acid.

MG FoamSan

MG FoamSan

Foaming Hand Sanitizer

* Kills >99.9% of Most Common Germs
* High Foaming Action
* Non-Drying & Moisturizing
* Alcohol & Fragrance Free
* Non-Flammable
* Effective in 15 Seconds

MG FoamSan is based on the active ingredient Benzalkonium Chloride and is effective in killing >99.9% of common germs. It does not dry or harm your skin. The unique instant foaming application dries quickly and leaves hands feeling soft. MG FoamSan does not contain alcohol or fragrance.

16oz

1Gallon

55 Gallons

275 Gallons

4x1

12x16

INGREDIENTS AND APPEARANCE

MG FOAMSAN 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50241-522
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)
ACETAMIDOETHOXYETHANOL (UNII: LVX2APC4XR)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50241-522-01	3785 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/26/2020
2	NDC: 50241-522-02	454 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/26/2020
3	NDC: 50241-522-03	24970 g in 1 DRUM; Type 0: Not a Combination Product	05/26/2020
4	NDC: 50241-522-04	124850 g in 1 DRUM; Type 0: Not a Combination Product	05/26/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/26/2020

Labeler - Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc. (028311595)

Registrant - Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc. (028311595)

Establishment
Name	Address	ID/FEI	Business Operations
Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.		028311595	manufacture(50241-522) , api manufacture(50241-522) , pack(50241-522)