FDA.reportPublic FDA data

NDC 57479-102 - POISON OAK AND IVY

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
57479-102
Package NDCs from labels
57479-102-01
Manufacturer
DeMartini Spring Hill Pharmacy, Inc. | Spa de Soleil
Effective date
2023-08-24
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
POISON OAK AND IVY - DeMartini Spring Hill Pharmacy, Inc. | Spa de SoleilDeMartini Spring Hill Pharmacy, Inc. | Spa de Soleil2023-08-24HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57479-102-012025-01-30C16284748780-12cef2736-67a1-d83d-e063-dadaa90ab31f03aeed00-2027-0b57-e063-6394a90a8b47

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57479-102-01POISON OAK AND IVY103 mL in 1 TUBEGEL1031

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57479-102POISON OAK AND IVY (HYDROCORTISONE, PHENOL) GEL [DEMARTINI SPRING HILL PHARMACY, INC.]11 package rows20230825_03aeed00-2027-0b57-e063-6394a90a8b47.zip