Home NDC 0316-0232 Zeasorb
Product NDC 0316-0232
11-digit product format 003160232
Labeler code 0316
Product ID 0316-0232_d88d4688-0022-e720-e053-2995a90a4d50
Type HUMAN OTC DRUG
Nonproprietary name miconazole nitrate
Dosage form POWDER
Route TOPICAL
Labeler Crown Laboratories
Application part333C
Marketing category OTC MONOGRAPH FINAL
Marketing start 2011-03-14
Marketing end 0000-00-00
Substance MICONAZOLE NITRATE
Active strength 20 mg/g
Pharmacologic classes Azole Antifungal [EPC], Azoles [CS]
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 0316-0232-25 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 0316-0232-25 f5e01cc5f278…a2eaf40c39c3…
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 0316-0232-25 00316023225 71 g in 1 BOTTLE (0316-0232-25) 71 g 2018-12-01 0000-00-00 No No Current