FDA.reportPublic FDA data

NDC 13985-009-15 - EnteDerm

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
13985-009
Requested NDC
13985-009-15
Package NDCs from labels
13985-009-75, 13985-009-15, 13985-009-30, 13985-009-40
Manufacturer
MWI | Med-Pharmex, Inc.
Effective date
1998-10-01
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 OintmentMWI | Med-Pharmex, Inc.1998-10-01PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Neomycin SulfateACTIVE INGREDIENT057Y626693ENTEDERM (NYSTATIN, NEOMYCIN SULFATE, THIOSTREPTON AND TRIAMCINOLONE ACETONIDE) OINTMENT [MWI]2
NystatinACTIVE INGREDIENTBDF1O1C72EENTEDERM (NYSTATIN, NEOMYCIN SULFATE, THIOSTREPTON AND TRIAMCINOLONE ACETONIDE) OINTMENT [MWI]2
ThiostreptonACTIVE INGREDIENTHR4S203Y18ENTEDERM (NYSTATIN, NEOMYCIN SULFATE, THIOSTREPTON AND TRIAMCINOLONE ACETONIDE) OINTMENT [MWI]2
Triamcinolone acetonideACTIVE INGREDIENTF446C597KAENTEDERM (NYSTATIN, NEOMYCIN SULFATE, THIOSTREPTON AND TRIAMCINOLONE ACETONIDE) OINTMENT [MWI]2
NeomycinACTIVE MOIETYI16QD7X297ENTEDERM (NYSTATIN, NEOMYCIN SULFATE, THIOSTREPTON AND TRIAMCINOLONE ACETONIDE) OINTMENT [MWI]2
NystatinACTIVE MOIETYBDF1O1C72EENTEDERM (NYSTATIN, NEOMYCIN SULFATE, THIOSTREPTON AND TRIAMCINOLONE ACETONIDE) OINTMENT [MWI]2
ThiostreptonACTIVE MOIETYHR4S203Y18ENTEDERM (NYSTATIN, NEOMYCIN SULFATE, THIOSTREPTON AND TRIAMCINOLONE ACETONIDE) OINTMENT [MWI]2
Triamcinolone acetonideACTIVE MOIETYF446C597KAENTEDERM (NYSTATIN, NEOMYCIN SULFATE, THIOSTREPTON AND TRIAMCINOLONE ACETONIDE) OINTMENT [MWI]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 13 of 34 · 663 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Triamcinolone AcetonideTRIAMCINOLONE ACETONIDEProPharma Distribution3edd3ad8-2561-59b5-e063-6294a90a01652025-09-15Warnings, Adverse reactionsExact identifier
unii: F446C597KA
Medi-First Triple AntibioticBACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATEUnifirst First Aid Corporationf2f0a1da-3e33-3c1a-e053-2a95a90a12b12025-09-09WarningsExact identifier
unii: 057Y626693
Ecolab Triple AntibioticBACITRACIN, NEOMYCIN SULFATE, POLYMYXIN B SULFATEEcolabs Food Safety Specialties, Inc.4aef8f98-db76-07f2-e054-00144ff8d46c2025-09-09WarningsExact identifier
unii: 057Y626693
Triple AntibioticBACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATEUnifirst First Aid Corporationd265f094-e654-4c68-9215-b5d061af885d2025-09-08WarningsExact identifier
unii: 057Y626693
Triple AntibioticBACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATEUnifirst First Aid Corporationd7c1a10e-c38d-4ae8-9a27-c07c2208ca842025-09-08WarningsExact identifier
unii: 057Y626693
Thompson Triple AntibioticBACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATEThompsonf883c4cb-c32c-76e3-e053-6294a90aa4fc2025-09-08WarningsExact identifier
unii: 057Y626693
Thompson Triple AntibioticBACITRACIN ZINC, POLYMYXIN B SULFATE, NEOMYCIN SULFATEThompsonde9489de-e677-2bd3-e053-2a95a90acfb42025-09-08WarningsExact identifier
unii: 057Y626693
Antibiotic Maximum StrengthBACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATEWalgreens9a092f24-65b2-4b57-8103-265ea3e033112025-09-02WarningsExact identifier
unii: 057Y626693
AerosootheTRIPLE ANTIBIOTIC OINTMENTAero Healthcare US LLC2287a31c-750c-728d-e054-00144ff88e882025-08-29WarningsExact identifier
unii: 057Y626693
Nystatin and Triamcinolone AcetonideNYSTATIN AND TRIAMCINOLONE ACETONIDEEncube Ethicals, Inc.d33829fc-86df-4e28-82c3-9dbcd8a9e28d2025-08-29Adverse reactionsExact identifier
unii: BDF1O1C72E
unii: F446C597KA
Triple Antibiotic Plus Pain ReliefBACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATEChain Drug Marketing Association Inc.3d4b3d73-171a-bc6a-e063-6394a90a69c12025-08-26WarningsExact identifier
unii: 057Y626693
NystopNYSTATINBryant Ranch Prepack69ebb4dd-f45d-448d-97cd-3f89354939752025-08-26Adverse reactionsExact identifier
unii: BDF1O1C72E
Dual Action CreamNEOMYCINSULFATE,POLYMYXINBSULFATE,PRAMOXINEHCLTrifecta Pharmaceutical USA LLCb84015ae-9c76-b1d7-e053-2a95a90a2cc82025-08-23WarningsExact identifier
unii: 057Y626693
Neomycin and Polymyxin B Sulfates and HydrocortisoneNEOMYCIN SULFATE, POLYMYXIN B SULFATE AND HYDROCORTISONESandoz Incff34da77-5e96-4ed1-8c28-ba0b2f35576a2025-08-20Warnings, Adverse reactionsExact identifier
unii: 057Y626693
nystatinNYSTATINBryant Ranch Prepacka5711dbe-f71c-435c-91f2-38c357532d182025-08-19Adverse reactionsExact identifier
unii: BDF1O1C72E
Neomycin Polymyxin B Sulfates and DexamethasoneNEOMYCIN SULFATE, POLYMYXIN B SULFATE AND DEXAMETHASONEPreferred Pharmaceuticals, Inc.449a6fd8-c2ac-40d0-b74a-e5c7fc6670f32025-08-18Warnings, Adverse reactionsExact identifier
unii: 057Y626693
Natureplex Antibiotic Plus Pain, Itch, Scar ReliefBACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDENatureplex LLCf0af8829-72fb-46b1-9328-6f4920710bb12025-08-15WarningsExact identifier
unii: 057Y626693
PROHEAL TRIPLE ANTIBIOTICBACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATENantong Health & Beyond Hygienic Products Inc.6c61d88e-4ced-4468-8f99-91652f7a03e42025-08-13WarningsExact identifier
unii: 057Y626693
TRIBIOTICBACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATEHART Healthc1903b9f-390a-4756-800c-fd93be4182e32025-08-13Warnings, Adverse reactionsExact identifier
unii: 057Y626693
Triple AntibioticBACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATEJ&A Digital Inc.9f006f16-083d-4e95-aec2-6ef83405f3932025-08-07WarningsExact identifier
unii: 057Y626693

Reported adverse events (FAERS/openFDA)#

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