FDA.reportPublic FDA data

NDC 17030-019 - Laxatone

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
17030-019
Package NDCs from labels
17030-019-25, 17030-019-42
Manufacturer
Vetoquinol USA, Inc. | Vetoquinol N.-A. INC
Effective date
2019-12-23
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Laxatone - Vetoquinol USA, Inc. | Vetoquinol N.-A. INCVetoquinol USA, Inc. | Vetoquinol N.-A. INC2019-12-23OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17030-019-25Laxatone70.9 g in 1 TUBEGEL70.93
17030-019-42Laxatone120.5 g in 1 TUBEGEL120.53

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17030-019LAXATONE (PETROLATUM AND MINERAL OIL) GEL [VETOQUINOL USA, INC.]32 package rows20191224_4bd7ff1b-8160-45fe-91a8-00c945ae3ca9.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Mineral OilACTIVE INGREDIENTT5L8T28FGPLAXATONE (PETROLATUM AND MINERAL OIL) GEL [VETOQUINOL USA, INC.]2
PetrolatumACTIVE INGREDIENT4T6H12BN9ULAXATONE (PETROLATUM AND MINERAL OIL) GEL [VETOQUINOL USA, INC.]2
Mineral OilACTIVE MOIETYT5L8T28FGPLAXATONE (PETROLATUM AND MINERAL OIL) GEL [VETOQUINOL USA, INC.]2
PetrolatumACTIVE MOIETY4T6H12BN9ULAXATONE (PETROLATUM AND MINERAL OIL) GEL [VETOQUINOL USA, INC.]2
Corn SyrupINACTIVE INGREDIENT9G5L16BK6NLAXATONE (PETROLATUM AND MINERAL OIL) GEL [VETOQUINOL USA, INC.]2
GelatinINACTIVE INGREDIENT2G86QN327LLAXATONE (PETROLATUM AND MINERAL OIL) GEL [VETOQUINOL USA, INC.]2
Maltose SyrupINACTIVE INGREDIENT00JKR0NZ8OLAXATONE (PETROLATUM AND MINERAL OIL) GEL [VETOQUINOL USA, INC.]2
MolassesINACTIVE INGREDIENTLSU3YX0KZOLAXATONE (PETROLATUM AND MINERAL OIL) GEL [VETOQUINOL USA, INC.]2
Sodium BenzoateINACTIVE INGREDIENTOJ245FE5EULAXATONE (PETROLATUM AND MINERAL OIL) GEL [VETOQUINOL USA, INC.]2
Soybean OilINACTIVE INGREDIENT241ATL177ALAXATONE (PETROLATUM AND MINERAL OIL) GEL [VETOQUINOL USA, INC.]2
WaterINACTIVE INGREDIENT059QF0KO0RLAXATONE (PETROLATUM AND MINERAL OIL) GEL [VETOQUINOL USA, INC.]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 39 of 39 · 762 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CVS Health Original SPF 15 Lip BalmOXYBENZONE, OCTINOXATE, PETROLATUMCVSe49680bd-bd61-40cf-abc8-51a1c88087262016-09-14WarningsExact identifier
unii: 4T6H12BN9U
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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