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Alclometasone Dipropionate

Alclometasone Dipropionate Cream USP, 0.05%Alclometasone Dipropionate Ointment USP, 0.05%

Approved
Approval ID

8db1bc33-3775-492a-927c-ee3b9abd79d6

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jul 27, 2011

Manufacturers
FDA

Physicians Total Care, Inc.

DUNS: 194123980

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Alclometasone Dipropionate

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code54868-2861
Application NumberANDA079061
Product Classification
M
Marketing Category
C73584
G
Generic Name
Alclometasone Dipropionate
Product Specifications
Route of AdministrationTOPICAL
Effective DateNovember 23, 2011
FDA Product Classification

INGREDIENTS (11)

ALCLOMETASONE DIPROPIONATEActive
Quantity: 0.5 mg in 1 g
Code: S56PQL4N1V
Classification: ACTIB
PROPYLENE GLYCOLInactive
Code: 6DC9Q167V3
Classification: IACT
CETOSTEARYL ALCOHOLInactive
Code: 2DMT128M1S
Classification: IACT
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATEInactive
Code: 593YOG76RN
Classification: IACT
PETROLATUMInactive
Code: 4T6H12BN9U
Classification: IACT
CHLOROCRESOLInactive
Code: 36W53O7109
Classification: IACT
PHOSPHORIC ACIDInactive
Code: E4GA8884NN
Classification: IACT
GLYCERYL MONOSTEARATEInactive
Code: 230OU9XXE4
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
CETETH-20Inactive
Code: I835H2IHHX
Classification: IACT
PEG-100 STEARATEInactive
Code: YD01N1999R
Classification: IACT

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Alclometasone Dipropionate - FDA Drug Approval Details