United States · FDA National Drug Code directory
Hydrocortisone Acetate Antipruritic (Anti-Itch)
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
- 51672-2069_44fe37d6-007d-8b3b-e063-6394a90ac802
- Product NDC
- 51672-2069
- Form
- CREAM
- Composition / generic term
- Hydrocortisone Acetate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20010601
- Source listing expiry
- 20261231
Source-listed ingredients
- HYDROCORTISONE ACETATE — 1 g/100g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (51672-2069-2) / 28.4 g in 1 TUBE · 51672-2069-2
- 454 g in 1 JAR (51672-2069-9) · 51672-2069-9
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.
Browse United States records →