Label: DESOXIMETASONE ointment
- NDC Code(s): 70771-1166-0, 70771-1166-1, 70771-1166-3
- Packager: Zydus Lifesciences Limited
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated November 5, 2022
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INGREDIENTS AND APPEARANCE
DESOXIMETASONE
desoximetasone ointmentProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:70771-1166 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DESOXIMETASONE (UNII: 4E07GXB7AU) (DESOXIMETASONE - UNII:4E07GXB7AU) DESOXIMETASONE 2.5 mg in 1 g Inactive Ingredients Ingredient Name Strength COCONUT OIL (UNII: Q9L0O73W7L) PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70771-1166-1 1 in 1 CARTON 12/05/2017 1 15 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:70771-1166-3 1 in 1 CARTON 12/05/2017 2 60 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC:70771-1166-0 1 in 1 CARTON 12/05/2017 3 100 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA205206 12/05/2017 Labeler - Zydus Lifesciences Limited (918596198) Registrant - Zydus Lifesciences Limited (918596198) Establishment Name Address ID/FEI Business Operations Zydus Lifesciences Limited 650650802 ANALYSIS(70771-1166) , MANUFACTURE(70771-1166)
