FDA.reportPublic FDA data

NDC 54925-003 - Derma-Vet

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
54925-003
Package NDCs from labels
54925-003-75, 54925-003-15, 54925-003-30, 54925-003-40
Manufacturer
Med-Pharmex, Inc.
Effective date
2023-05-26
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Nystatin, Neomycin Sulfate, Thiostrepton and Triamcinolone Acetonide OintmentMed-Pharmex, Inc.2023-05-26PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Neomycin SulfateACTIVE INGREDIENT057Y626693DERMA-VET (NYSTATIN, NEOMYCIN SULFATE, THIOSTREPTON AND TRIAMCINOLONE ACETONIDE) OINTMENT [MED-PHARMEX, INC.]3
NystatinACTIVE INGREDIENTBDF1O1C72EDERMA-VET (NYSTATIN, NEOMYCIN SULFATE, THIOSTREPTON AND TRIAMCINOLONE ACETONIDE) OINTMENT [MED-PHARMEX, INC.]3
ThiostreptonACTIVE INGREDIENTHR4S203Y18DERMA-VET (NYSTATIN, NEOMYCIN SULFATE, THIOSTREPTON AND TRIAMCINOLONE ACETONIDE) OINTMENT [MED-PHARMEX, INC.]3
Triamcinolone acetonideACTIVE INGREDIENTF446C597KADERMA-VET (NYSTATIN, NEOMYCIN SULFATE, THIOSTREPTON AND TRIAMCINOLONE ACETONIDE) OINTMENT [MED-PHARMEX, INC.]3
NeomycinACTIVE MOIETYI16QD7X297DERMA-VET (NYSTATIN, NEOMYCIN SULFATE, THIOSTREPTON AND TRIAMCINOLONE ACETONIDE) OINTMENT [MED-PHARMEX, INC.]3
NystatinACTIVE MOIETYBDF1O1C72EDERMA-VET (NYSTATIN, NEOMYCIN SULFATE, THIOSTREPTON AND TRIAMCINOLONE ACETONIDE) OINTMENT [MED-PHARMEX, INC.]3
ThiostreptonACTIVE MOIETYHR4S203Y18DERMA-VET (NYSTATIN, NEOMYCIN SULFATE, THIOSTREPTON AND TRIAMCINOLONE ACETONIDE) OINTMENT [MED-PHARMEX, INC.]3
Triamcinolone acetonideACTIVE MOIETYF446C597KADERMA-VET (NYSTATIN, NEOMYCIN SULFATE, THIOSTREPTON AND TRIAMCINOLONE ACETONIDE) OINTMENT [MED-PHARMEX, INC.]3

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 34 of 34 · 671 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Triamcinolone AcetonideTRIAMCINOLONE ACETONIDEProficient Rx LPe5e3a38d-717d-4412-80d3-7130100add0a2020-09-01Adverse reactionsExact identifier
unii: F446C597KA
KENALOG-40TRIAMCINOLONE ACETONIDEAsclemed USA, Inc.0bc9c75f-963c-40b0-995b-dfcbd50371a52020-05-06Warnings, Adverse reactionsExact identifier
unii: F446C597KA
NystatinNYSTATIN OINTMENTProficient Rx LP711950c4-1889-4acd-ab76-9a16176ce1e42020-03-01Adverse reactionsExact identifier
unii: BDF1O1C72E
Triamcinolone AcetonideTRIAMCINOLONE ACETONIDEProficient Rx LP41c1fe93-0509-4cf6-ac35-049028b731de2019-12-01Adverse reactionsExact identifier
unii: F446C597KA
NystatinNYSTATINProficient Rx LP5ef15e1c-66dc-4858-8552-d83e42c3883e2019-11-01Adverse reactionsExact identifier
unii: BDF1O1C72E
NYSTATINNYSTATINLeading Pharma, LLC8900ba02-2c6a-4dd4-b82f-45620c06e2552019-09-19Adverse reactionsExact identifier
unii: BDF1O1C72E
Nystatin Topical PowderNYSTATIN TOPICAL POWDEREpic Pharma, LLC7f313a3b-7a4c-47fb-ad9f-e267514db5272018-05-02Adverse reactionsExact identifier
unii: BDF1O1C72E
Water-Jel 3-in-1 AntibioticBACITRACIN ZINC, POLYMYXIN B SULFATE, NEOMYCIN SULFATEWater-Jel Technologiesd5fcaffd-af38-4285-a79c-6df7424c76fa2017-11-16WarningsExact identifier
unii: 057Y626693
Triamcinolone AcetonideTRIAMCINOLONE ACETONIDEGlenmark Pharmaceuticals Inc., USA8c380328-127b-4ca6-bf56-ef461e7044712017-08-22Adverse reactionsExact identifier
unii: F446C597KA
CVS Triple AntibioticBACITRACIN, NEOMYCIN, POLYMYXIN BCVS Pharmacy454bfeed-f58f-003a-e054-00144ff8d46c2017-01-04WarningsExact identifier
unii: 057Y626693
Triamcinolone AcetonideTRIAMCINOLONE ACETONIDEGlenmark Pharmaceuticals Inc., USAa9b3764d-fd3d-4fcc-8d22-5aa848da1b062016-07-11Adverse reactionsExact identifier
unii: F446C597KA

Reported adverse events (FAERS/openFDA)#

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