# Pramosone

NDC: 54766-763
Generic name: hydrocortisone acetate and pramoxine hydrochloride
Labeler / Manufacturer: Sebela Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Unapproved drug (not FDA-reviewed)
Dosage form: OINTMENT
Routes: TOPICAL
Marketing started: 20260526



## Active ingredients

- HYDROCORTISONE ACETATE: 10 mg/g
- PRAMOXINE HYDROCHLORIDE: 10 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"54766-763"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=54766-763
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d4d85400-3bb3-11e5-830e-0002a5d5c51b