MG DermaGel 70

Manufacturer: Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.
Effective date: 2025-12-23
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 01:28:24

Label at a glance#

ProductMG DermaGel 70

Active ingredientALCOHOL

Label structure10 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin Recommended for repeated use

Dosage and administration

Place a small amount of MG Dermagel 70 in your palm to throughly cover your hands. Rub hands together briskly until dry. Keep out of reach of children. For children under 6, use only under adult supervison. Not recommended for infants.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol....70%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

DOSAGE & ADMINISTRATION SECTION

For hand sanitizing to decrease bacteria on the skin
Recommended for repeated use

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 Dermagel 70 in your palm to throughly cover your hands.
Rub hands together briskly until dry.
Keep out of reach of children. For children under 6, use only under adult supervison. Not recommended for infants.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water
Isopropyl Alcohol
Glycerin
Propylene Glycol
Carbomer
Triisopropanolamine

MG DermaGel 70

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	3
581662	ethanol 0.7 ML/ML Topical Gel	SCD	3
581662	ethanol 70 % Topical Gel	SY	3
581662	ethyl alcohol 70 % Topical Gel	SY	3

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Data code	QR Code	URL:https://morgan-gallacher.com/wp-content/uploads/2020/04/MG-DermaGel-62_EN.pdf		MG_1G_DermaGel 70_31JAN2024.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
50241-465-02	MG DermaGel 70	208.198 L in 1 DRUM	LIQUID	208.198		3
50241-465-04	MG DermaGel 70	3.785 L in 1 BOTTLE, PLASTIC	LIQUID	3.785		3

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

MG DermaGel 70
Ethyl Alcohol
WATER
GLYCERIN
PROPYLENE GLYCOL
TRIISOPROPANOLAMINE
CARBOMER HOMOPOLYMER TYPE A
ISOPROPYL ALCOHOL
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
50241-465	50241-465-02, 50241-465-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
TRIISOPROPANOLAMINE	W9EN9DLM98	IACT
CARBOMER HOMOPOLYMER TYPE A	F68VH75CJC	IACT
ISOPROPYL ALCOHOL	ND2M416302	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

Source XML

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
MG DermaGel 70	ETHYL ALCOHOL	Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.	56ac723b-3ede-4c94-bf4a-0572a7b42b59	2025-12-23	Warnings	Exact identifier ndc (package): 50241-465-04 ndc (package): 50241-465-02 ndc (product): 50241-465 ndc11 (package): 50241046504 ndc11 (package): 50241046502 spl id: 2137c9e5-1035-4dd7-ab26-2575acc3df61 spl set id: 56ac723b-3ede-4c94-bf4a-0572a7b42b59

Reported adverse events (FAERS/openFDA)#

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