MG DERMAFOAM- 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 DermaFoam

ACTIVE INGREDIENT

Benzalkonium Chloride ...........0.13%

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. Do not ingest.

- Stop use and contact a doctor if irritation or redness develops

  or if conditions persist.

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

-Apply small amount of product to wet hands.

-Work into lather and rinse thoroughly, and dry hands.

Inactive Ingredients

Water, Cocamidopropyl Betaine, Caprylyl Glucoside, Glycerine, Tetrasodium EDTA, Benzisothiazol, Methylisothiozol, Fragrance, Citric Acid, Aloe Vera, Yellow #5, Red #40

MG DermaFoam

image description
MG DERMAFOAM 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50241-339
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
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
GLYCERIN (UNII: PDC6A3C0OX)  
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
EDETATE SODIUM (UNII: MP1J8420LU)  
WATER (UNII: 059QF0KO0R)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50241-339-021 in 1 BOX09/25/2018
1NDC:50241-339-013.80564 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 other09/25/2018
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(50241-339) , api manufacture(50241-339) , pack(50241-339)

Revised: 12/2023
Document Id: 009bc8f3-d98d-464d-8c53-4f8cdacc2ad9
Set id: 4a43a605-f333-4c76-a476-476a9cc2e13a
Version: 10
Effective Time: 20231221
 
Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.