Corti-Sav

Product NDC
80587-101
11-digit product format
805870101
Labeler code
80587
Product ID
80587-101_d8e12be1-af11-68f6-e053-2995a90a7782
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hydrocortisone 1% Iodoquinol
Dosage form
CREAM
Route
TOPICAL
Labeler
Prime Labs LLC DBA Quality CDMO
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2020-06-01
Marketing end
0000-00-00
Substance
HYDROCORTISONE; IODOQUINOL
Active strength
10 mg/g; mg/g
Pharmacologic classes
Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
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 dateDatasetScopePackage NDCSnapshotSource SHA-256
2024-10-04 04:10 UTC · source 2024-10-03excluded productproduct367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-03excluded packagepackage80587-101-01367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09excluded productproduct557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-09excluded packagepackage80587-101-01557ba5c1ecfa…9c80585c8c6e…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
80587-101-018058701010128.4 g in 1 TUBE (80587-101-01) 28.4 g2020-06-010000-00-00NoNoCurrent