Home NDC 79073-003 natouch
Product NDC 79073-003
11-digit product format 790730003
Labeler code 79073
Product ID 79073-003_552104ad-64de-5474-e063-6294a90ac405
Type HUMAN OTC DRUG
Nonproprietary name miconazole
Dosage form SOAP
Route TOPICAL
Labeler Natouch LLC
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-02-01
Substance MICONAZOLE
Active strength 1.2 g/120g
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 natouch
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MICONAZOLE 1.2 g/120g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 7NNO0D7S5M Internal UNII 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 8 of 51 · 1,004 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 79073-003-04 79073000304 120 g in 1 BOX (79073-003-04) 120 g 2022-08-01 No No Current