Home NDC 51672-5330-01 NDC 51672-5330-01 - Hydrocortisone with Aloe This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 51672-5330
Requested NDC 51672-5330-01
Package NDCs from labels 51672-5330-1, 51672-5330-2, 51672-5330-3, 51672-5330-01
Manufacturer NuCare Pharmaceuticals, Inc.
Effective date 2026-06-24
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 51672-5330-1 Hydrocortisonewith Aloe 1 in 1 CARTON CREAM 1 2 51672-5330-1 Hydrocortisonewith Aloe 14.2 g in 1 TUBE CREAM 14.2 2 51672-5330-2 Hydrocortisonewith Aloe 28.4 g in 1 TUBE CREAM 28.4 2 51672-5330-2 Hydrocortisonewith Aloe 1 in 1 CARTON CREAM 1 2 51672-5330-3 Hydrocortisonewith Aloe 1 in 1 CARTON CREAM 1 2 51672-5330-3 Hydrocortisonewith Aloe 60 g in 1 TUBE CREAM 60 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51672-5330 HYDROCORTISONE WITH ALOE (HYDROCORTISONE CREAM 1%) CREAM [TARO PHAMACEUTICALS U.S.A., INC.] 1 Current NDC, 6 package rows 20250331_312ddc8d-100e-cfac-e063-6294a90acd09.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 56 of 174 · 3,467 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.