Home NDC 60232-0046 Private Label Antifungal Barrier Cream
Product NDC 60232-0046
11-digit product format 602320046
Labeler code 60232
Product ID 60232-0046_05322d7d-55e0-47ae-aa76-58f346e44c4e
Type HUMAN OTC DRUG
Nonproprietary name miconazole nitrate antifungal cream
Dosage form CREAM
Route TOPICAL
Labeler Swiss-American CDMO, LLC
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-05-09
Substance MICONAZOLE NITRATE
Active strength 200 g/1000g
Pharmacologic classes Azole Antifungal [EPC], Azoles [CS]
NDC exclude flag No
Listing certified through 2026-12-31
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 Private Label Antifungal Barrier Cream
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MICONAZOLE NITRATE 200 g/1000g
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 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 60232-0046-1 Private Label Antifungal Barrier Cream 85 g in 1 TUBE CREAM 85 1
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 8 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 60232-0046-1 60232004601 85 g in 1 TUBE (60232-0046-1) 85 g 2025-05-09 No No Current