FDA.reportPublic FDA data

Marquis Gel Formula

Manufacturer
Marquis XT LLC
Effective date
2024-01-29
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:12:18

Label at a glance#

ProductMarquis Gel Formula
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under the 6 years of age when using this product to avoid sswallowing.

Label contents#

Full prescribing information#

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product on hands to cover all surfaces. Rub hands together until dry.

Supervise children under the 6 years of age when using this product to avoid sswallowing.

Warnings

WARNINGS SECTION

FOr extenal use only. Flammable. Keep away from heat or flame.

Do not use

in children less than 2 months of age

on open skin wounds

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These maybe signs of a serious condition.

Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

In active ingredients

INACTIVE INGREDIENT SECTION

Glycerin, Isopropyl myristate, methacrylic acid, Propylene glycol, Purified USP water, Tetrahydroxypropyl ethylenediamine, vitamin E

Use[s]

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease. FOr use when soap and water are not available.

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 76585-002-14NDC 76585-002-14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76585-002MARQUIS GEL FORMULA GEL [MARQUIS XT LLC]4Legacy NDC20240130_a7569ad0-a9b0-326b-e053-2a95a90a3c17.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76585-00276585-002-14, 76585-002-17, 76585-002-11, 76585-002-13, 76585-002-15, 76585-002-12, 76585-002-18, 76585-002-16, 76585-002-20

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
NameUNIIKind
ALCOHOL3K9958V90MACTIB
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (4500 MPA.S)T967IEU43CIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
EDETOLQ4R969U9FRIACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
39e9925d-f99d-5612-e063-6394a90ac4aba7569ad0-a9b0-326b-e053-2a95a90a3c172025-07-14WarningsExact identifier
spl set id: a7569ad0-a9b0-326b-e053-2a95a90a3c17

Reported adverse events (FAERS/openFDA)#

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