Home NDC 48951-3124 Copper Oxide 0.4
Product NDC 48951-3124
11-digit product format 489513124
Labeler code 48951
Product ID 48951-3124_389362be-d335-f00c-e063-6294a90a61b6
Type HUMAN OTC DRUG
Nonproprietary name Copper Oxide 0.4
Dosage form OINTMENT
Route TOPICAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance CUPRIC OXIDE
Active strength 1 [hp_X]/g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Copper Oxide 0.4
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CUPRIC OXIDE 1 [hp_X]/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination V1XJQ704R4 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48951-3124-5 Copper Oxide 0.4 60 g in 1 TUBE OINTMENT 60 5
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-3124 COPPER OXIDE 0.4 OINTMENT [URIEL PHARMACY INC.] 4 Current NDC, Legacy NDC, 1 package rows 20240111_3987be95-ba66-4f2e-9255-351d799ac304.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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 48951-3124-5 48951312405 60 g in 1 TUBE (48951-3124-5) 60 g 2009-09-01 0000-00-00 No No Current