Marquis Gel Formula by Marquis Extraction Technology LLC MARQUIS GEL FORMULA gel

Marquis Gel Formula by

Drug Labeling and Warnings

Marquis Gel Formula by is a Otc medication manufactured, distributed, or labeled by Marquis Extraction Technology LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Directions

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

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

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

Use[s]

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

Active Ingredients

Alcohol 70% v/v

Purpose

Antiseptic

keep out of reach of children

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MARQUIS GEL FORMULA 
marquis gel formula gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76585-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (4500 MPA.S) (UNII: T967IEU43C)	4 mL  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	1 mL  in 100 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)	0.5 mL  in 100 mL
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)	0.005 mL  in 100 mL
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)	0.1 mL  in 100 mL
EDETOL (UNII: Q4R969U9FR)	0.75 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76585-002-14	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2020	12/31/2021
2	NDC: 76585-002-17	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2020	12/31/2021
3	NDC: 76585-002-11	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2020	12/31/2021
4	NDC: 76585-002-13	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2020	12/31/2021
5	NDC: 76585-002-15	12113 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2020	12/31/2021
6	NDC: 76585-002-12	1040875 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2020	12/31/2021
7	NDC: 76585-002-18	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2020	12/31/2021
8	NDC: 76585-002-16	18927 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2020	12/31/2021
9	NDC: 76585-002-20	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	06/01/2020

Labeler - Marquis XT LLC (117496233)

Establishment
Name	Address	ID/FEI	Business Operations
Marquis XT LLC		117496233	manufacture(76585-002)