FDA.reportPublic FDA data

NDC 0091-0695 - Cortifoam

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
0091-0695
Package NDCs from labels
0091-0695-20
Manufacturer
Schwarz Pharma
Effective date
2007-02-27
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Cortifoam - Schwarz PharmaSchwarz Pharma2007-02-27Human prescription drug label

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
hydrocortisone acetateACTIVE INGREDIENT3X7931PO74CORTIFOAM (HYDROCORTISONE ACETATE) AEROSOL, FOAM [SCHWARZ PHARMA]2
hydrocortisoneACTIVE MOIETYWI4X0X7BPJCORTIFOAM (HYDROCORTISONE ACETATE) AEROSOL, FOAM [SCHWARZ PHARMA]2
cetyl alcoholINACTIVE INGREDIENT936JST6JCNCORTIFOAM (HYDROCORTISONE ACETATE) AEROSOL, FOAM [SCHWARZ PHARMA]2
emulsifying waxINACTIVE INGREDIENTCORTIFOAM (HYDROCORTISONE ACETATE) AEROSOL, FOAM [SCHWARZ PHARMA]2
isobutaneINACTIVE INGREDIENTBXR49TP611CORTIFOAM (HYDROCORTISONE ACETATE) AEROSOL, FOAM [SCHWARZ PHARMA]2
methylparabenINACTIVE INGREDIENTCORTIFOAM (HYDROCORTISONE ACETATE) AEROSOL, FOAM [SCHWARZ PHARMA]2
polyoxyethylene-10-stearyl etherINACTIVE INGREDIENTCORTIFOAM (HYDROCORTISONE ACETATE) AEROSOL, FOAM [SCHWARZ PHARMA]2
propaneINACTIVE INGREDIENTCORTIFOAM (HYDROCORTISONE ACETATE) AEROSOL, FOAM [SCHWARZ PHARMA]2
propylene glycolINACTIVE INGREDIENT6DC9Q167V3CORTIFOAM (HYDROCORTISONE ACETATE) AEROSOL, FOAM [SCHWARZ PHARMA]2
propylparabenINACTIVE INGREDIENTZ8IX2SC1OHCORTIFOAM (HYDROCORTISONE ACETATE) AEROSOL, FOAM [SCHWARZ PHARMA]2
trolamineINACTIVE INGREDIENT9O3K93S3TKCORTIFOAM (HYDROCORTISONE ACETATE) AEROSOL, FOAM [SCHWARZ PHARMA]2
waterINACTIVE INGREDIENT059QF0KO0RCORTIFOAM (HYDROCORTISONE ACETATE) AEROSOL, FOAM [SCHWARZ PHARMA]2

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 1 of 1 ยท 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
7152A68F-1BA9-7555-4FBF-9A69741CD1B436F623DF-2AE3-4858-9783-C058097951F42007-02-27Warnings, Adverse reactionsExact identifier
spl id: 7152A68F-1BA9-7555-4FBF-9A69741CD1B4
spl set id: 36F623DF-2AE3-4858-9783-C058097951F4

Reported adverse events (FAERS/openFDA)#

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