Home NDC 22431-359-01 NDC 22431-359-01 - Relief Soothing Bath Treatment 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 22431-359
Requested NDC 22431-359-01
Package NDCs from labels 22431-359-01, 22431-359-02, 22431-359-03
Manufacturer Blue Cross Laboratories, Inc.
Effective date 2022-11-15
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Soothing Bath Treatment Blue Cross Laboratories, Inc. 2022-11-15 HUMAN OTC DRUG LABEL
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 22431-359-01 Relief Soothing Bath Treatment 42.5 g in 1 PACKET GRANULE, EFFERVESCENT 42.5 24 22431-359-02 Relief Soothing Bath Treatment 6 in 1 BOX GRANULE, EFFERVESCENT 6 24 22431-359-03 Relief Soothing Bath Treatment 3 in 1 BOX GRANULE, EFFERVESCENT 3 24
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 22431-359 RELIEF SOOTHING BATH TREATMENT (COLLOIDAL OATMEAL) GRANULE, EFFERVESCENT [BLUE CROSS LABORATORIES, INC.] 24 Legacy NDC, 3 package rows 20221116_d8deb0ff-1d5f-41e3-919f-d6c4ef9810ce.zip
DailyMed Socrata Ingredients# 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 7 of 12 · 235 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.