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Pramosone

NDC 54766-763 · HUMAN PRESCRIPTION DRUG · OINTMENT

Generic namehydrocortisone acetate and pramoxine hydrochloride
Labeler / ManufacturerSebela Pharmaceuticals Inc.
Marketing categoryUnapproved drug (not FDA-reviewed)
Dosage form / routeOINTMENT · TOPICAL
Active ingredientsHYDROCORTISONE ACETATE (10 mg/g)
PRAMOXINE HYDROCHLORIDE (10 mg/g)
Marketing started20260526
Package count0

External sources

Source: openFDA. Public-domain (CC0).