MARQUIS GEL FORMULA- marquis gel formula gel 
Marquis XT LLC

----------

Active Ingredients

Alcohol 70% v/v

Purpose Antiseptic

Purpose

Antiseptic

Stop use and ask a doctor if

irritation or rash occurs. These may be signs of a serious condition.

Use

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

For use when soap and water are unavailable.

Warnings

For external use only.

Keep away from heat or flame.

Do not use

in children less than 2 months of age

on open skin wounds

in eyes

When using this product

keep out of eyes, ears, and mouth

in case of contactwith eyes, rinse eyes thoroughly with water

Kep out of reach of children

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

Directions

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

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

Other Information

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

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

Inactive Ingredients

acrylate copolymer, aloe, denatonium benzoate, fragrance, propylene glycol, water

Package Label

0100

Gel 010

MARQUIS GEL FORMULA 
marquis gel formula gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76585-010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
LINALOOL, (+)- (UNII: F4VNO44C09) 0.3 mL  in 100 mL
DENATONIUM BENZOATE ANHYDROUS (UNII: M5BA6GAF1O) 0.00035 mL  in 100 mL
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (4500 MPA.S) (UNII: T967IEU43C) 1.1 mL  in 100 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.005 mL  in 100 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 1 mL  in 100 mL
CUMINYL ACETALDEHYDE (UNII: WSW8QXE6HG) 0.3 mL  in 100 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76585-010-173785 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
2NDC:76585-010-11473 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
3NDC:76585-010-13236 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
4NDC:76585-010-14946 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
5NDC:76585-010-1512113 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
6NDC:76585-010-121040875 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
7NDC:76585-010-18355 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
8NDC:76585-010-1618927 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
9NDC:76585-010-2059 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00310/01/2020
Labeler - Marquis XT LLC (117496233)
Establishment
NameAddressID/FEIBusiness Operations
Marquis XT LLC117496233manufacture(76585-010)

Revised: 1/2024
Document Id: 101bb6be-f771-d92f-e063-6394a90a0872
Set id: afd8c2d9-4c04-2129-e053-2a95a90a29d3
Version: 3
Effective Time: 20240129
 
Marquis XT LLC