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
54766-729_4314aef2-c610-9ee4-e063-6394a90ae0ca
Product NDC
54766-729
Form
LOTION
Composition / generic term
hydrocortisone acetate and pramoxine hydrochloride
Labeler
Sebela Pharmaceuticals Inc.
Marketing category
ANDA
Marketing start / end (source format)
20150702 / 20261231

Source-listed ingredients

  • HYDROCORTISONE ACETATE — 10 mg/mL
  • PRAMOXINE HYDROCHLORIDE — 10 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 118 mL in 1 BOTTLE (54766-729-04) · 54766-729-04

Source and coverage

Open FDA National Drug Code directory

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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Pramosone — United States | Molindra Medicines