FDA.reportPublic FDA data

MG DermaSan 72

Manufacturer
Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.
Effective date
2025-12-23
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 01:28:30

Label at a glance#

ProductMG DermaSan 72
Active ingredientISOPROPYL ALCOHOL
Label structure10 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin

Dosage and administration

Place a small amount of MG DermaSan 72 in your palm to throughly cover your hands.  Rub hands together briskly until dry.  For children under 6 years of age should be supervised when using this product. 

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol....72%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

DOSAGE & ADMINISTRATION SECTION

  • For hand sanitizing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

  • For external use only.
  • Flammable keep away from fire or flame

When using this product

WARNINGS AND PRECAUTIONS SECTION

  • Avoid contact with eyes. In case of eye contract, flush eyes with water. 

Stop use and ask doctor if

WARNINGS AND PRECAUTIONS SECTION

  • irritation or redness develops, if condition persists for more than 72 hours.  

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Conrol Center right away

Directions

INDICATIONS & USAGE SECTION

  • Place a small amount of MG DermaSan 72 in your palm to throughly cover your hands. 
  • Rub hands together briskly until dry. 
  • For children under 6 years of age should be supervised when using this product. 

Inactive Ingredients

INACTIVE INGREDIENT SECTION

  • Water
  • Glycerin
  • Propylene Glycol

MG DermaSan 72

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2287034isopropyl alcohol 72 % Topical GelPSN9
2287034isopropyl alcohol 0.72 ML/ML Topical GelSCD9
2287034isopropyl alcohol 72 % Topical GelSY9

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130850018773065GTIN-13: 0850018773065
EAN-13: 0850018773065
GTIN-12: 850018773065
UPC-A: 850018773065
GTIN storage (14 digits): 00850018773065		MG_1G_DermaSan 72_A22.jpg
Data codeQR CodeURL:https://morgan-gallacher.com/wp-content/uploads/2020/04/MG-DermaSan-72_EN.pdfMG_1G_DermaSan 72_A22.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50241-330-01MG DermaSan 723.785 L in 1 JUGGEL3.7859
50241-330-02MG DermaSan 724 in 1 BOXGEL49
50241-330-07MG DermaSan 72208.198 L in 1 DRUMGEL208.1989

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50241-33050241-330-01, 50241-330-02, 50241-330-07

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
TRIISOPROPANOLAMINEW9EN9DLM98IACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ISOPROPYL ALCOHOLND2M416302ACTIB

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MG DermaSan 72ISOPROPYL ALCOHOLMorgan Gallacher Inc. DBA Custom Chemical Formulators Inc.cccdefbc-09ef-417f-9b7a-1b254ae6e4382025-12-23WarningsExact identifier
ndc (package): 50241-330-07
ndc (package): 50241-330-02
ndc (package): 50241-330-01
ndc (product): 50241-330
ndc11 (package): 50241033007
ndc11 (package): 50241033002
ndc11 (package): 50241033001
spl id: 4050dfc2-165d-42b4-963b-7ec9c5b15bec
spl set id: cccdefbc-09ef-417f-9b7a-1b254ae6e438

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.