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FDA Approval

Hydrocortisone Acetate Pramoxine Hydrochloride

CompanyPageview Pharmaceuticals (DUNS: 117003305)

Effective Date

February 1, 2022

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Hydrocortisone acetate(25 mg in 1 1)

Hydrocortisone Acetate/Pramoxine Hydrochloride(18 mg in 1 1)

Products (1)

Hydrocortisone Acetate Pramoxine Hydrochloride

NDC Product Code

73028-401

Route of Administration

RECTAL

Effective Date

February 1, 2022

Ingredients

Hydrocortisone acetateActive

Code: 3X7931PO74Class: ACTIBQuantity: 25 mg in 1 1

Hydrocortisone Acetate/Pramoxine HydrochlorideActive

Code: 88AYB867L5Class: ACTIBQuantity: 18 mg in 1 1

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