Home NDC 87786-021 DRAVYNOR BALANITIS RELIEF Cream
Product NDC 87786-021
11-digit product format 877860021
Labeler code 87786
Product ID 87786-021_56b76a52-0744-4fe6-e063-6294a90a98a8
Type HUMAN OTC DRUG
Nonproprietary name Miconazole Nitrate 2% BALANITIS RELIEF Cream
Dosage form CREAM
Route TOPICAL
Labeler Wenzhou Yuyuan Pharmaceutical Co., Ltd.
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-16
Substance MICONAZOLE NITRATE
Active strength 2 g/100mL
Pharmacologic classes Azole Antifungal [EPC], Azoles [CS]
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 DRAVYNOR BALANITIS RELIEF Cream
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MICONAZOLE NITRATE 2 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination VW4H1CYW1K Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 998483 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 23 of 49 · 973 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87786-021-01 87786002101 30 mL in 1 BOTTLE (87786-021-01) 30 ml 2026-07-16 No No Current