OTC Medication Information: MG DermaWash

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.

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, Caprylyl/Capryl Gluciside, Citric Acid, Cocamide MIPA, Cocamidopropyl Betaine, Glycerin, Lauryl Polyglucose, Magnesium Nitrate, Maltodextrin, Methylchloroisothiazolinone, Methylthiazolinone, PEG
150 Distearate, Tetrasodium EDTA, Water

MG DermaWash

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MG DERMAWASH
benzalkonium chloride liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:50241-302
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 13 kg in 100 kg
Inactive Ingredients
Ingredient Name Strength
ALOE VERA FLOWER
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE
ANHYDROUS CITRIC ACID
COCO MONOISOPROPANOLAMIDE
COCAMIDOPROPYL BETAINE
GLYCERIN
LAURYL GLUCOSIDE
MAGNESIUM NITRATE
MALTODEXTRIN
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
PEG-150 DISTEARATE
EDETATE SODIUM
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50241-302-02 1 BOTTLE, PLASTIC in 1 BOX contains a BOTTLE, PLASTIC (50241-302-01)
1 NDC:50241-302-01 3.80564 kg in 1 BOTTLE, PLASTIC This package is contained within the BOX (50241-302-02)
2 NDC:50241-302-03 210.25 kg in 1 DRUM None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 09/24/2018
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 Operations
Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc. 028311595 manufacture (50241-302), api manufacture (50241-302), pack (50241-302)

Revised: 12/2023 Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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