Active Ingredient
Benzalkonium Chloride......0.13%
Mg Dermawash Liquid
FDA Label NDC 50241-302
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Morgan Gallacher Inc. Dba Custom Chemical Formulators Inc. for the product Mg Dermawash (NDC 50241-302). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, when using this product, keep out of reach of children., directions, inert ingredients:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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
* Please review the disclaimer below.
