Home NDC 53997-002-01 NDC 53997-002-01 - Lansinoh Anti-itch 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 53997-002
Requested NDC 53997-002-01
Package NDCs from labels 53997-002-01, 53997-002-02
Manufacturer Lansinoh Laboratories Inc | Dhaliwal Pharmaceuticals Laboratories, LLC
Effective date 2024-12-22
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Lansinoh Anti Itch Lansinoh Laboratories Inc | Dhaliwal Pharmaceuticals Laboratories, LLC 2024-12-22 HUMAN OTC DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 53997-002-01 Lansinoh Anti-itch 125 mL in 1 TUBE CREAM 125 2 53997-002-02 Lansinoh Anti-itch 1 in 1 CARTON CREAM 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 53997-002 LANSINOH ANTI-ITCH (MENTHOL 0.5%) CREAM [LANSINOH LABORATORIES INC] 2 2 package rows 20241224_19357c7f-b7fa-dacc-e063-6394a90ad1c1.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 37 of 224 · 4,461 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.