Mometasone Furoate

Basic Information

Product Name

Mometasone Furoate

FDA Product Code

68071-1538

Regulatory Information

NDC Product Code

68071-1538

Application Number

ANDA078541

Marketing Category

C73584

Effective Date

February 11, 2021

Territorial Authority

USA

FDA Title

These highlights do not include all the information needed to use safely and effectively. See full prescribing information for . Initial U.S. Approval: 1987

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Version Number

Active Ingredients

HEXYLENE GLYCOL

Code: KEH0A3F75J

Class Code: IACT

PHOSPHORIC ACID

Code: E4GA8884NN

Class Code: IACT

WHITE WAX

Code: 7G1J5DA97F

Class Code: IACT

POLYOXYL 20 CETOSTEARYL ETHER

Code: YRC528SWUY

Class Code: IACT

PROPYLENE GLYCOL STEARATE

Code: MZM1I680W0

Class Code: IACT

STEARYL ALCOHOL

Code: 2KR89I4H1Y

Class Code: IACT

PETROLATUM

Code: 4T6H12BN9U

Class Code: IACT

TITANIUM DIOXIDE

Code: 15FIX9V2JP

Class Code: IACT

WATER

Code: 059QF0KO0R

Class Code: IACT

ALUMINUM STARCH OCTENYLSUCCINATE

Code: I9PJ0O6294

Class Code: IACT

MOMETASONE FUROATE

Quantity: 1 mg in 1 g

Code: 04201GDN4R

Class Code: ACTIB

Active Moieties

MOMETASONE

Code: 8HR4QJ6DW8

Basic Information

Regulatory Information

Company Information

Active Ingredients

HEXYLENE GLYCOL

PHOSPHORIC ACID

WHITE WAX

POLYOXYL 20 CETOSTEARYL ETHER

PROPYLENE GLYCOL STEARATE

STEARYL ALCOHOL

PETROLATUM

TITANIUM DIOXIDE

WATER

ALUMINUM STARCH OCTENYLSUCCINATE

Active Moieties

MOMETASONE