FDA.reportPublic FDA data

NDC 15878-413 - UDDER BALM

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
15878-413
Package NDCs from labels
15878-413-13, 15878-413-18
Manufacturer
H. W. Naylor Company Inc.
Effective date
2013-01-04
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
UDDER BALMH. W. Naylor Company Inc.2013-01-04OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
15878-413-13UDDER BALM255 g in 1 CANOINTMENT2553
15878-413-18UDDER BALM1200 g in 1 CANOINTMENT12003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
15878-413UDDER BALM (OXYQUINOLINE) OINTMENT [H. W. NAYLOR COMPANY INC.]32 package rows20130504_2907f343-4457-bf36-2e0b-aa074e63a4bd.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
OxyquinolineACTIVE INGREDIENT5UTX5635HPUDDER BALM (OXYQUINOLINE) OINTMENT [H. W. NAYLOR COMPANY INC.]3
OxyquinolineACTIVE MOIETY5UTX5635HPUDDER BALM (OXYQUINOLINE) OINTMENT [H. W. NAYLOR COMPANY INC.]3
.beta.-caroteneINACTIVE INGREDIENT01YAE03M7JUDDER BALM (OXYQUINOLINE) OINTMENT [H. W. NAYLOR COMPANY INC.]3
ApocarotenalINACTIVE INGREDIENTV22N3E2U32UDDER BALM (OXYQUINOLINE) OINTMENT [H. W. NAYLOR COMPANY INC.]3
Clove Leaf OilINACTIVE INGREDIENTVCA5491KVFUDDER BALM (OXYQUINOLINE) OINTMENT [H. W. NAYLOR COMPANY INC.]3
Isopropyl AlcoholINACTIVE INGREDIENTND2M416302UDDER BALM (OXYQUINOLINE) OINTMENT [H. W. NAYLOR COMPANY INC.]3
LanolinINACTIVE INGREDIENT7EV65EAW6HUDDER BALM (OXYQUINOLINE) OINTMENT [H. W. NAYLOR COMPANY INC.]3
ParaffinINACTIVE INGREDIENTI9O0E3H2ZEUDDER BALM (OXYQUINOLINE) OINTMENT [H. W. NAYLOR COMPANY INC.]3
PetrolatumINACTIVE INGREDIENT4T6H12BN9UUDDER BALM (OXYQUINOLINE) OINTMENT [H. W. NAYLOR COMPANY INC.]3
Sodium BorateINACTIVE INGREDIENT91MBZ8H3QOUDDER BALM (OXYQUINOLINE) OINTMENT [H. W. NAYLOR COMPANY INC.]3
WaterINACTIVE INGREDIENT059QF0KO0RUDDER BALM (OXYQUINOLINE) OINTMENT [H. W. NAYLOR COMPANY INC.]3
Yellow WaxINACTIVE INGREDIENT2ZA36H0S2VUDDER BALM (OXYQUINOLINE) OINTMENT [H. W. NAYLOR COMPANY 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 54 of 72 · 1,440 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
First Aid Only Alcohol Antiseptic PadALCOHOL PADAcme United Corporation55421010-d806-4ca4-e054-00144ff88e882024-11-26WarningsExact identifier
unii: ND2M416302
Wipesplus Hand Sanitizing WipesISOPRPOYL ALCOHOLAcme United Corporatione7272bea-04ac-59c2-e053-2a95a90a2e0c2024-11-26WarningsExact identifier
unii: ND2M416302
First Aid Only Sting Relief PadBENZOCAINE, ISOPROPYL ALCOHOLAcme United Corporationd71047f6-1353-c758-e053-2995a90a962c2024-11-26WarningsExact identifier
unii: ND2M416302
First Aid Only Hand Sanitizing WipeISOPROPYL ALCOHOLAcme United Corporation03ec9021-816f-970c-e063-6294a90a67322024-11-26WarningsExact identifier
unii: ND2M416302
PhysiciansCare Ophthalmic Solution EyewashPURIFIED WATER 98.3%Acme United Corporationcca454e0-b2bd-4215-bc06-426fcc3f7bd62024-11-26WarningsExact identifier
unii: 059QF0KO0R
PhysiciansCare Ophthalmic Solution EyewashPURIFIED WATER 98.3%Acme United Corporationd3812fa3-9334-464d-b50c-98548ff767272024-11-26WarningsExact identifier
unii: 059QF0KO0R
DANGTTEOLMINERAL WATERAQBC CO., LTD27db14a9-3812-433f-e063-6394a90a11e72024-11-26WarningsExact identifier
unii: 059QF0KO0R
Lil Drug Store Petroleum JellyPETROLATUMLil Drug Store Products, Inca8a56786-20c3-43c1-a4db-8502ff08e4cb2024-11-25WarningsExact identifier
unii: 4T6H12BN9U
First Aid Only Alcohol Antiseptic PadISOPROPYL ALCOHOLAcme United Coporationa01fec1b-1339-40b9-e053-2995a90aeda52024-11-23WarningsExact identifier
unii: ND2M416302
Med-Nap Sterile Alcohol Prep PadsISOPROPYL ALCOHOLAcme United Corporationc6eff57b-d537-69c8-e053-2a95a90adc3a2024-11-23WarningsExact identifier
unii: ND2M416302
First Aid Only Alcohol AntisepticISOPROPYL ALCOHOLAcme United Corporationa810e723-ad0c-8c71-e053-2995a90a0acc2024-11-23WarningsExact identifier
unii: ND2M416302
Universal 50% Rubbing AlcoholISOPROPYL ALCOHOLUniversal Distribution Center LLC0dcc9bd2-aea5-4c27-9956-47d56221726b2024-11-22WarningsExact identifier
unii: ND2M416302
Universal 70% Rubbing Alcohol with Wintergreen and GlycerinISOPROPYL ALCOHOLUniversal Distribution Center LLC9a9d42ad-79d5-4acc-b5d9-cb7468961d472024-11-22WarningsExact identifier
unii: ND2M416302
Universal 50% Rubbing Alcohol with Wintergreen and GlycerinISOPROPYL ALCOHOLUniversal Distribution Center LLC044a6287-f568-4cfa-a813-7fc0e6ffc3522024-11-22WarningsExact identifier
unii: ND2M416302
NEXXGEN 70% RUBBING ALCOHOLISOPROPYL ALCOHOLA & A Nexxgen LLCce73ac48-c5af-4a35-950c-62ff0232aa302024-11-22WarningsExact identifier
unii: ND2M416302
Universal 70% Rubbing AlcoholISOPROPYL ALCOHOLUniversal Distribution Center LLCd8b9b0e7-2cb8-4fc5-af55-790e64d6cfe82024-11-22WarningsExact identifier
unii: ND2M416302
Isopropyl AlcoholISOPROPYL ALCOHOLMazza Healthcare, LLCee83ba9f-ac65-48b7-9f84-5be6fec9a9092024-11-21WarningsExact identifier
unii: ND2M416302
Alcohol sterileISOPROPYL ALCOHOLCardinal Health, Incbb7c530f-5d80-4158-b715-09c1c837299d2024-11-21WarningsExact identifier
unii: ND2M416302
Sting Relief PadBENZOCAINE, ISOPROPYL ALCOHOLChangzhou Maokang Medical Products Co., Ltd1936c5f4-274b-8e49-e063-6394a90ac6422024-11-21WarningsExact identifier
unii: ND2M416302
Alcohol sterileISOPROPYL ALCOHOLCardinal Health 200 LLC10135db9-f614-4511-96ac-faa6a02a1b612024-11-21WarningsExact identifier
unii: ND2M416302

Reported adverse events (FAERS/openFDA)#

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