Home NDC 87021-602 Urea 39
Product NDC 87021-602
11-digit product format 870210602
Labeler code 87021
Product ID 87021-602_c298ff83-acc1-4dcd-8eb9-2b2d3a57439c
Type HUMAN OTC DRUG
Nonproprietary name Urea
Dosage form CREAM
Route TOPICAL
Labeler Krewe Pharma, LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2026-06-02
Substance UREA
Active strength 390 mg/g
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Urea 39
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength UREA 390 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 8W8T17847W Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1093289 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 Sample Exclude flag Status 87021-602-04 87021060204 1 JAR in 1 JAR (87021-602-04) / 113 g in 1 JAR 1 jar 2026-06-02 No No Current