United States · FDA National Drug Code directory
Pramosone
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 54766-777_52fa7b5f-1e33-3070-e063-6394a90afc13
- Product NDC
- 54766-777
- Form
- OINTMENT
- Composition / generic term
- hydrocortisone acetate and pramoxine hydrochloride
- Labeler
- Sebela Pharmaceuticals Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 20260526
- Source listing expiry
- 20271231
Source-listed ingredients
- HYDROCORTISONE ACETATE — 25 mg/g
- PRAMOXINE HYDROCHLORIDE — 10 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 28.4 g in 1 TUBE (54766-777-04) · 54766-777-04
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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