MG DERMAWASH- benzalkonium chloride liquid 
Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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MG DermaWash

ACTIVE INGREDIENT

Benzalkonium Chloride......0.13%

Purpose

Antiseptic

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.

-  Do not ingest. Stop use and contact a doctor if irritation or

    redness develop or conditions persist.

Keep out of reach of children.

If swallowed, get medical help

or contact Poison Control Center right away. 

Directions

- Apply small amount of product to wet hands.

- Work into lather and rinse thogoughly. Dry hands.

INERT INGREDIENTS:

Aloe Barbadensis Leaf Juice, Benzisothiazol,

Caprylyl Glucoside, Citric Acid, Cocamide MIPA, Cocamidopropyl
Betaine, Glycerine, Lauryl Glucoside, Maltodextrin, Methylisathiozol, PEG
150 Distearate, Tetrasodium EDTA, Water

MG DermaWash

MG DermaWash

image description

MG DERMAWASH 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50241-302
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE13 kg  in 100 kg
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)  
CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)  
GLYCERIN (UNII: PDC6A3C0OX)  
DITETRACYCLINE TETRASODIUM EDETATE (UNII: WX0A0IT7K5)  
BENZISOTHIAZOLINONE (UNII: HRA0F1A4R3)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50241-302-021 in 1 BOX09/24/2018
1NDC:50241-302-013.80564 kg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other09/24/2018
Labeler - Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc. (028311595)
Registrant - Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc. (028311595)
Establishment
NameAddressID/FEIBusiness Operations
Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.028311595manufacture(50241-302) , api manufacture(50241-302) , pack(50241-302)

Revised: 12/2022
 
Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.