Home NDC 70000-0679 Antifungal Powder
Product NDC 70000-0679
11-digit product format 700000679
Labeler code 70000
Product ID 70000-0679_5d69762f-d5f3-bfe5-e063-6394a90a9894
Type HUMAN OTC DRUG
Nonproprietary name Miconazole Nitrate
Dosage form POWDER
Route TOPICAL
Labeler LEADER/ Cardinal Health 110, Inc.
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-08-16
Substance MICONAZOLE NITRATE
Active strength 20 mg/g
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 Antifungal Powder
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MICONAZOLE NITRATE 20 mg/g
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70000-0679-1 Antifungal Powder 71 g in 1 BOTTLE, PLASTIC POWDER 71 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70000-0679 ANTIFUNGAL POWDER (MICONAZOLE NITRATE) POWDER [LEADER/ CARDINAL HEALTH 110, INC.] 2 Current NDC, 1 package rows 20241103_1fcf072b-cf12-967a-e063-6294a90acfc7.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 8 of 49 · 973 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 70000-0679-1 70000067901 71 g in 1 BOTTLE, PLASTIC (70000-0679-1) 71 g 2024-08-16 No No Current