FDA.reportPublic FDA data

Marquis Gel Formula

Manufacturer
Marquis Extraction Technology | Marquis Extraction Technology LLC
Effective date
2020-07-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:30:11

Label at a glance#

ProductMarquis Gel Formula
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

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

Storage and handling

Store between 59-86F (15-30C) Avoid freezing and excessive heat above 104F (40C)

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v Purpose Antisepic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin that potentially can cause disease

For use when soap and water are unavailable

Warnings

WARNINGS SECTION

For external use only

Flammable

Keep away from heat or flame

D not use

OTC - DO NOT USE SECTION

in children less than 2 months of age

on open skin wounds

in eyes

When using this product

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

irritation or rash occurs, these may be signs of a serious condition

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

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

Other Information

STORAGE AND HANDLING SECTION

Store between 59-86F (15-30C)

Avoid freezing and excessive heat above 104F (40C)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

acrylates copolymer, aloe barbadensis (aloe vera) leaf juice, fragrance, glycerin, isopropyl myristate, propylene glysol, triilsopropanolamine, water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Gel 008Gel 008

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76585-008-112022-01-28C16284748780-1d6a99b39-e324-a426-e053-dadaa90af4c2ae4565c3-5ab8-800d-e053-2a95a90ae172
76585-008-122022-01-28C16284748780-1d6a99b39-e324-a426-e053-dadaa90af4c2ae4565c3-5ab8-800d-e053-2a95a90ae172
76585-008-132022-01-28C16284748780-1d6a99b39-e324-a426-e053-dadaa90af4c2ae4565c3-5ab8-800d-e053-2a95a90ae172
76585-008-142022-01-28C16284748780-1d6a99b39-e324-a426-e053-dadaa90af4c2ae4565c3-5ab8-800d-e053-2a95a90ae172
76585-008-152022-01-28C16284748780-1d6a99b39-e324-a426-e053-dadaa90af4c2ae4565c3-5ab8-800d-e053-2a95a90ae172
76585-008-162022-01-28C16284748780-1d6a99b39-e324-a426-e053-dadaa90af4c2ae4565c3-5ab8-800d-e053-2a95a90ae172
76585-008-172022-01-28C16284748780-1d6a99b39-e324-a426-e053-dadaa90af4c2ae4565c3-5ab8-800d-e053-2a95a90ae172
76585-008-182022-01-28C16284748780-1d6a99b39-e324-a426-e053-dadaa90af4c2ae4565c3-5ab8-800d-e053-2a95a90ae172
76585-008-202022-01-28C16284748780-1d6a99b39-e324-a426-e053-dadaa90af4c2ae4565c3-5ab8-800d-e053-2a95a90ae172

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76585-008-11Marquis Gel Formula473 mL in 1 BOTTLEGEL4731
76585-008-12Marquis Gel Formula1040875 mL in 1 BOTTLEGEL10408751
76585-008-13Marquis Gel Formula236 mL in 1 BOTTLEGEL2361
76585-008-14Marquis Gel Formula946 mL in 1 BOTTLEGEL9461
76585-008-15Marquis Gel Formula12113 mL in 1 BOTTLEGEL121131
76585-008-16Marquis Gel Formula18927 mL in 1 BOTTLEGEL189271
76585-008-17Marquis Gel Formula3785 mL in 1 BOTTLEGEL37851
76585-008-18Marquis Gel Formula355 mL in 1 BOTTLEGEL3551
76585-008-20Marquis Gel Formula59 mL in 1 BOTTLEGEL591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76585-008MARQUIS GEL FORMULA GEL [MARQUIS EXTRACTION TECHNOLOGY]1Legacy NDC, 9 package rows20200925_ae4565c3-5ab8-800d-e053-2a95a90ae172.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76585-00876585-008-17, 76585-008-11, 76585-008-13, 76585-008-14, 76585-008-15, 76585-008-12, 76585-008-18, 76585-008-16, 76585-008-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
CUMINYL ACETALDEHYDEWSW8QXE6HGIACT
GLYCERINPDC6A3C0OXIACT
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (4500 MPA.S)T967IEU43CIACT
LINALOOL, (+)-F4VNO44C09IACT
TRIISOPROPYLAMINEY67CF9Z56LIACT
ALCOHOL3K9958V90MACTIB
ALOE VERA LEAFZY81Z83H0XIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
DENATONIUM BENZOATE ANHYDROUSM5BA6GAF1OIACT

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
ae4565c3-5ab9-800d-e053-2a95a90ae172ae4565c3-5ab8-800d-e053-2a95a90ae1722020-07-01WarningsExact identifier
spl id: ae4565c3-5ab9-800d-e053-2a95a90ae172
spl set id: ae4565c3-5ab8-800d-e053-2a95a90ae172

Reported adverse events (FAERS/openFDA)#

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