Home NDC 0135-0195-08 NDC 0135-0195-08 - NICODERM CQ 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 0135-0195
Requested NDC 0135-0195-08
Package NDCs from labels 0135-0195-02, 0135-0195-03, 0135-0195-08, 0135-0195-05
Manufacturer Haleon US Holdings LLC
Effective date 2025-07-14
Current FDA listing Not matched in FDA.report NDC product tables FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0135-0195-02 NICODERMCQ 24 h in 1 PATCH PATCH, EXTENDED RELEASE 24 14 0135-0195-02 NICODERMCQ 14 in 1 CARTON PATCH, EXTENDED RELEASE 14 14 0135-0195-03 NICODERMCQ 1 in 1 PACKAGE PATCH, EXTENDED RELEASE 1 14 0135-0195-03 NICODERMCQ 21 in 1 CARTON PATCH, EXTENDED RELEASE 21 14 0135-0195-05 NICODERMCQ 14 in 1 CARTON PATCH, EXTENDED RELEASE 14 14 0135-0195-08 NICODERMCQ 24 h in 1 PATCH PATCH, EXTENDED RELEASE 24 14
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0135-0195 NICODERM CQ (NICOTINE) PATCH, EXTENDED RELEASE [HALEON US HOLDINGS LLC] 13 Current NDC, Legacy NDC, 6 package rows 20250519_93b2d1b9-83c1-40b5-b6af-90c38c8d6cef.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 6 of 32 · 629 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.