Home NDC 11673-830 NDC 11673-830 - Daytime Severe and Nighttime Severe cold and flu 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 11673-830
Manufacturer TARGET CORPORATION | TIME CAP LABORATORIES, INC. | MARKSANS PHARMA LIMITED
Effective date 2024-06-21
Current FDA listing Not matched in FDA.report NDC product tables
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 130 of 384 · 7,674 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Circle K Daytime Cold and Flu ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE Lil' Drug Store Products, Inc. b6a46498-d9a8-4da2-9283-57d135f305a5 2025-12-23 Warnings Exact identifier application number: M012 unii: 9D2RTI9KYH unii: 04JA59TNSJ unii: 362O9ITL9D Acetaminophen ACETAMINOPHEN CVS PHARMACY INC bd8ce39f-ccf8-3976-e053-2a95a90abb1f 2025-12-23 Warnings Exact identifier unii: 362O9ITL9D Circle K Nighttime Cold and Flu ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND DOXYLAMINE SUCCINATE Lil' Drug Store Products, Inc. 7c5faec2-28c6-4c15-a268-d8b578140b74 2025-12-23 Warnings Exact identifier application number: M012 unii: 9D2RTI9KYH unii: V9BI9B5YI2 unii: 362O9ITL9D Acetaminophen ACETAMINOPHEN PUBLIX SUPERMARKETS, INC 08f5af1d-365b-a97c-e063-6394a90a99ae 2025-12-23 Warnings Exact identifier unii: 362O9ITL9D Sugar Free Honey Lemon Cough Drops MENTHOL Walmart 67650b94-adbb-87fb-e053-2a91aa0a87e6 2025-12-23 Warnings Exact identifier application number: M012 Equate Benz-Dex Cough and Throat Lozenges BENZOCAINE Walmart c0a6cb7f-a247-e610-e053-2a95a90a4199 2025-12-23 Warnings Exact identifier application number: M012 unii: 9D2RTI9KYH Equate Honey Lemon Cough Drops MENTHOL WalMart 0028be18-5162-ff51-e063-6294a90ae517 2025-12-23 Warnings Exact identifier application number: M012 Equate SF Menthol Cough Drops MENTHOL WalMart 003a229c-b014-e9f3-e063-6294a90aa5ed 2025-12-23 Warnings Exact identifier application number: M012 Equate Menthol Cough Drops MENTHOL Walmart 124e6968-f59c-39d4-e063-6294a90a66d4 2025-12-23 Warnings Exact identifier application number: M012 Equate Severe Menthol Throat Drop MENTHOL Walmart 125f3f5a-52aa-e398-e063-6394a90a0012 2025-12-23 Warnings Exact identifier application number: M012 Equate Menthol Chewable Gels MENTHOL Walmart 1ba4b2be-7242-0a23-e063-6294a90af29c 2025-12-23 Warnings Exact identifier application number: M012 Walgreens Severe Menthol Throat Drops MENTHOL Walgreens 21dd3c68-cbc6-4799-e063-6394a90a6972 2025-12-23 Warnings Exact identifier application number: M012 cherry throat relief lozenges BENZOCAINE Zee Medical 499d0748-538f-678c-e054-00144ff8d46c 2025-12-23 Warnings Exact identifier application number: M012 Guaiasorb DM DEXTROMETHORPHAN HBR, GUAIFENESIN NuCare Pharmaceuticals, Inc. 46a480c7-7092-b809-e063-6294a90a60cd 2025-12-23 Warnings Exact identifier application number: M012 unii: 9D2RTI9KYH unii: 495W7451VQ menthol cough drops MENTHOL Winco Foods 360a6304-206d-5475-e054-00144ff8d46c 2025-12-23 Warnings Exact identifier application number: M012 menthol cough drops MENTHOL Winco Foods 36342d8c-34ab-6178-e054-00144ff8d46c 2025-12-23 Warnings Exact identifier application number: M012 cherry cough drops MENTHOL Winco Foods 37244333-1307-5121-e054-00144ff8d46c 2025-12-23 Warnings Exact identifier application number: M012 honey lemon cough drops MENTHOL Winco foods 37718c73-880e-4a5c-e054-00144ff8d46c 2025-12-23 Warnings Exact identifier application number: M012 honey lemon cough drops MENTHOL Winco Foods 40676ddc-577f-5cc9-e054-00144ff88e88 2025-12-23 Warnings Exact identifier application number: M012 Sugar Free Menthol Cough Drops MENTHOL Winco Foods 3788e8b6-ab9e-1513-e054-00144ff88e88 2025-12-23 Warnings Exact identifier application number: M012
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.