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 24 of 72 · 1,440 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Vis Guard Lubricant EyeOintment PMMINERAL OIL, WHITE PETROLATUM OINTMENTUlai Health LLC1040a92b-d342-a9fd-e063-6294a90a45ef2026-01-13WarningsExact identifier
unii: 4T6H12BN9U
WISH ISOPROPYL ALCOHOLWISH ISOPROPYL ALCOHOLClick Products LLC484befce-ecfe-5514-e063-6294a90a169c2026-01-13WarningsExact identifier
unii: ND2M416302
WISH RUBBING ALCOHOL 32ozWISH RUBBING ALCOHOL 32OZ 70%CLICK PRODUCTS LLC4836b564-0b8c-2fb4-e063-6394a90a9c4a2026-01-13WarningsExact identifier
unii: ND2M416302
LONAZEMMENTHOL,PETROLATUMPEER PHARM LTD.91f7a741-4178-4639-9cd5-746a4b9a21bf2026-01-12WarningsExact identifier
unii: 4T6H12BN9U
Isopropyl Alcohol 50%ISOPROPYL ALCOHOL 50%Hydrox Laboratories930bb3a3-5ca3-414c-b4fb-c71ee17fc7462026-01-12WarningsExact identifier
unii: ND2M416302
Isopropyl AlcoholISOPROPYL ALCOHOLHydrox Laboratoriesf2f07464-6bd5-434c-8dea-0ba659c0e5492026-01-12WarningsExact identifier
unii: ND2M416302
Isopropyl Alcohol with Wintergreen 70%ISOPROPYL ALCOHOL WITH WINTERGREEN 70%Hydrox Laboratories5845f723-8866-4738-bec6-621041899f572026-01-12WarningsExact identifier
unii: ND2M416302
Isopropyl AlcoholISOPROPYL ALCOHOLHydrox Laboratories2042cf29-52c5-4f1e-aae6-78e025994d182026-01-12WarningsExact identifier
unii: ND2M416302
Isopropyl Alcohol with Wintergreen 50%ISOPROPYL ALCOHOL WITH WINTERGREEN 50%Hydrox Laboratories3a15a900-2b48-487f-b252-a1a1e0d0abfc2026-01-12WarningsExact identifier
unii: ND2M416302
Isopropyl Rubbing AlcoholISOPROPYL ALCOHOLDiscount Drug Mart37a6c0fb-e9c4-4a95-9539-ca5766b3a7012026-01-12WarningsExact identifier
unii: ND2M416302
Isopropyl AlcoholISOPROPYL ALCOHOLDiscount Drug Mart7ac6b062-b471-4653-9d6f-de2ca8f8b0142026-01-12WarningsExact identifier
unii: ND2M416302
Isopropyl Rubbing AlcoholISOPROPYL ALCOHOLEpic Medical Supply Corp.88e6418c-ceb3-4bd6-8765-b476d8bf3ff32026-01-12WarningsExact identifier
unii: ND2M416302
Alcohol Prep PadsISOPROPYL ALCOHOLNINGBO TIANBO FIRST AID PRODUCT CO., LTD.3cce065a-0254-43ad-a96f-aae6979997be2026-01-12WarningsExact identifier
unii: ND2M416302
SolidagoSOLIDAGO VIRGAUREA, UVA-URSI, PAREIRA BRAVA, SABAL SERRULATA, POPULUS TREMULOIDES, STAPHYSAGRIA, CANTHARIS, TEREBINTHIA, BORAXMarco Pharma International LLC.915727a5-78d9-4865-ad35-8a10cce014ca2026-01-12WarningsExact identifier
unii: 91MBZ8H3QO
Sooth-a-StingBENZOCAINE, ISOPROPYL ALCOHOLHART Healthc0e7d661-a9c9-4656-a516-57552848ebe82026-01-12WarningsExact identifier
unii: ND2M416302
HCS Alcohol Prep Pad LargeISOPROPYL ALCOHOLConcordance Healthcare Solutions, LLC.3c4b14ca-3ff1-4a55-a239-31bfb5b3aaa52026-01-12WarningsExact identifier
unii: ND2M416302
AlcoholISOPROPYL ALCOHOLHART Health8d01b10b-7916-420e-9d44-ebd3806fe3152026-01-12WarningsExact identifier
unii: ND2M416302
Grandma ElsDIAPER RASH OINTMENTABBE Laboratories, Inc.b331c46d-855f-45f5-b3ee-3a611370face2026-01-10WarningsExact identifier
unii: 7EV65EAW6H
unii: 4T6H12BN9U
Quality Choice Isopropyl Alcohol WipesISOPROPYL ALCOHOLChain Drug Marketing Association, Inc.b58145c6-0f6c-5a47-e053-2995a90a5d7f2026-01-09WarningsExact identifier
unii: ND2M416302
YeastCalmSODIUM BORATE,CALENDULA OFFICINALIS FLOWERING TOP,CANDIDA ALBICANS,GOLDENSEALLaboratoires Boirdoncd384b93-b803-8810-e053-2a95a90acdf02026-01-09WarningsExact identifier
unii: 91MBZ8H3QO

Reported adverse events (FAERS/openFDA)#

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