Active Ingredient
Benzalkonium Chloride ...........0.13%
Mg Dermafoam Liquid
FDA Label NDC 50241-339
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 Dermafoam (NDC 50241-339). 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, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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
MG DermaFoam
* Please review the disclaimer below.
