Home NDC 69036-220 NDC 69036-220 - SALLUS Pain Relief Collection with Naproxen 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 69036-220
Package NDCs from labels 69036-220-30
Manufacturer Sallus Laboratories, Llc | Glenmark Pharmaceuticals Limited | Integrated Pharma Solutions LLC
Effective date 2016-02-03
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type SALLUS Pain Relief Collection Sallus Laboratories, Llc | Glenmark Pharmaceuticals Limited | Integrated Pharma Solutions LLC 2016-02-03 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69036-220-30 SALLUS Pain Relief Collection with Naproxen 30 in 1 BOTTLE TABLET 30 500 mg 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69036-220 SALLUS PAIN RELIEF COLLECTION WITH NAPROXEN (NAPROXEN) KIT [SALLUS LABORATORIES, LLC] 2 Unmatched 20160203_96aced89-fe07-439a-ac4c-59a0969993eb.zip
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 90 of 156 · 3,106 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.