Label: MARQUIS GEL FORMULA gel
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NDC Code(s):
76585-010-11,
76585-010-12,
76585-010-13,
76585-010-14, view more76585-010-15, 76585-010-16, 76585-010-17, 76585-010-18, 76585-010-20
- Packager: Marquis XT LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 29, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Stop use and ask a doctor if
- Use
- Warnings
- Do not use
- When using this product
- Kep out of reach of children
- Directions
- Other Information
- Inactive Ingredients
- Package Label
-
INGREDIENTS AND APPEARANCE
MARQUIS GEL FORMULA
marquis gel formula gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76585-010 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 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:76585-010-17 3785 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2020 2 NDC:76585-010-11 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2020 3 NDC:76585-010-13 236 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2020 4 NDC:76585-010-14 946 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2020 5 NDC:76585-010-15 12113 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2020 6 NDC:76585-010-12 1040875 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2020 7 NDC:76585-010-18 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2020 8 NDC:76585-010-16 18927 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2020 9 NDC:76585-010-20 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 10/01/2020 Labeler - Marquis XT LLC (117496233) Establishment Name Address ID/FEI Business Operations Marquis XT LLC 117496233 manufacture(76585-010)