Home NDC 48951-8371 Renes 5X
Product NDC 48951-8371
11-digit product format 489518371
Labeler code 48951
Product ID 48951-8371_49df5018-3e16-ef32-e063-6394a90a4ddc
Type HUMAN OTC DRUG
Nonproprietary name Renes 5X
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance PORK KIDNEY
Active strength 5 [hp_X]/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Renes 5X
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PORK KIDNEY 5 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination X7BCI5P86H Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48951-8371-1 Renes 5X 1 mL in 1 AMPULE LIQUID 1 4 48951-8371-1 Renes 5X 10 in 1 BOX LIQUID 10 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-8371 RENES 5X LIQUID [URIEL PHARMACY INC.] 3 Current NDC, Legacy NDC, 2 package rows 20250127_b713c3d6-c854-14d0-e053-2995a90ad71c.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 48951-8371-1 48951837101 10 AMPULE in 1 BOX (48951-8371-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 0000-00-00 No No Current