Home NDC 72288-357-00 NDC 72288-357-00 - basic care daytime severe cold and flu nighttime 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 72288-357
Requested NDC 72288-357-00
Package NDCs from labels 72288-357-00, 72288-357-62
Manufacturer Amazon.com Services LLC
Effective date 2024-11-15
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72288-357-00 basic care daytime severe cold and flu nighttime cold and flu 2 in 1 BLISTER PACK TABLET, FILM COATED 32 10 mg 4 72288-357-00 basic care daytime severe cold and flu nighttime severe cold and flu 2 in 1 BLISTER PACK TABLET, FILM COATED 16 5 mg 3 72288-357-62 basic care daytime severe cold and flu 2 in 1 BLISTER PACK TABLET, FILM COATED 2 3 72288-357-62 basic care daytime severe cold and flu 12 in 1 CARTON TABLET, FILM COATED 12 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72288-357 BASIC CARE DAYTIME SEVERE COLD AND FLU NIGHTTIME COLD AND FLU (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, DOXYLAMINE SUCCINATE) KIT [AMAZON.COM SERVICES LLC] 4 Current NDC, Legacy NDC 20241116_298d2796-5ae5-4346-b6d2-2ced2dd29dc3.zip 72288-357 BASIC CARE DAYTIME SEVERE COLD AND FLU (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE) TABLET, FILM COATED [AMAZON.COM SERVICES LLC] 3 Current NDC, Legacy NDC, 2 package rows 20241109_50528d29-ce8c-4efb-a86c-17246b017db0.zip 72288-357 BASIC CARE DAYTIME SEVERE COLD AND FLU NIGHTTIME SEVERE COLD AND FLU (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, DOXYLAMINE SUCCINATE) KIT [AMAZON.COM SERVICES LLC] 3 Current NDC, Legacy NDC 20241116_9f4daadb-fdaf-4ea9-bad9-7ed9f8cee7f2.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 6 of 450 · 8,995 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Afrin Original Nasal OXYMETAZOLINE HYDROCHLORIDE JC World Bell Wholesale Co., Inc. ecfa14b8-a3f3-4569-b489-c9e1a51cf09e 2026-08-31 Warnings Exact identifier application number: M012 Dextromethorphan HBr DEXTROMETHORPHAN HBR BIONPHARMA INC. 5a5dde85-8785-8149-e063-6294a90a4d57 2026-08-31 Warnings Exact identifier application number: M012 unii: 9D2RTI9KYH Equate Nasal OXYMETAZOLINE HCL Sixarp, LLC 5a5e2458-bab0-4931-e063-6394a90ad606 2026-08-31 Warnings Exact identifier application number: M012 MUCINEX INSTASOOTHE SORE THROAT PLUS COUGH RELIEF DEXTROMETHORPHAN HYDROBROMIDE AND HEXYLRESORCINOL Reckitt Benckiser LLC 8d670d91-9e22-45b9-b568-5b62c2133d32 2026-08-31 Warnings Exact identifier application number: M012 unii: 9D2RTI9KYH Daytime Cold and Flu Multi Symptom Relief ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL Shield Pharmaceuticals Corp e85b4c2a-d4e0-452c-9a08-fcc0ff6eaa21 2026-08-31 Warnings Exact identifier application number: M012 unii: 9D2RTI9KYH unii: 04JA59TNSJ unii: 362O9ITL9D MAX relief junior Grape CHILDRENS ACETAMINOPHEN Akron Pharma Inc. cc769c26-556a-4831-bd75-61a7383aa707 2026-08-31 Warnings Exact identifier unii: 362O9ITL9D MAX relief junior CHILDRENS ACETAMINOPHEN Akron Pharma Inc. ebb3b4ba-2d0b-48d9-b6ee-6d4696aea047 2026-08-31 Warnings Exact identifier unii: 362O9ITL9D Daytime Cold and Flu Maximum Strength ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL Shield Pharmaceuticals Corp 67849e09-2056-4013-98b1-d003ed3250a2 2026-08-31 Warnings Exact identifier application number: M012 unii: 9D2RTI9KYH unii: 04JA59TNSJ unii: 362O9ITL9D MAX relief junior ACETAMINOPHEN Akron Pharma Inc. 0e43b885-3843-4f11-9a53-02a38c228313 2026-08-31 Warnings Exact identifier unii: 362O9ITL9D MAX relief junior CHILDREN ACETAMINOPHEN Akron Pharma Inc. d7874e4d-0b38-4bb1-9a62-aa4f66d9baf9 2026-08-31 Warnings Exact identifier unii: 362O9ITL9D MAX relief junior Grape CHILDREN ACETAMINOPHEN Akron Pharma Inc. 3c7a7f40-4963-4fd1-942e-93fa08a45830 2026-08-31 Warnings Exact identifier unii: 362O9ITL9D Genexa Kids Pain and Fever ACETAMINOPHEN Genexa Inc. 5a615118-33c9-1520-e063-6394a90a21a6 2026-08-31 Warnings Exact identifier unii: 362O9ITL9D MAX Tussin Mucus and Chest Congestion Sugar Free GUAIFENESIN Akron Pharma Inc. 3b023b91-e703-4599-9864-96d8c328b45c 2026-08-31 Warnings Exact identifier application number: M012 unii: 495W7451VQ MAX Tussin Mucus and Chest Congestion GUAIFENESIN Akron Pharma Inc. ac874a31-5556-4669-937f-dcb52aaecd8a 2026-08-31 Warnings Exact identifier application number: M012 unii: 495W7451VQ MAX Tussin Cough and Chest Congestion DM DEXTROMETHORPHAN HBR, GUAIFENESIN Akron Pharma Inc. e0ce4287-bfa1-4413-97c8-4fe2e39bda36 2026-08-31 Warnings Exact identifier application number: M012 unii: 9D2RTI9KYH unii: 495W7451VQ Acetaminophen PM Extra Strength ACETAMINOPHEN, DIPHENHYDRAMINE HCL United Natural Foods, Inc. dba UNFI 24173e77-92ec-4a87-a471-d6867837c180 2026-08-31 Warnings Exact identifier application number: M012 unii: 362O9ITL9D Mucinex DM GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE Select Consumer Group 3c9c8fb0-8a00-4b0f-e063-6394a90af632 2026-08-30 Warnings Exact identifier unii: 9D2RTI9KYH unii: 495W7451VQ Allergy Relief DIPHENHYDRAMINE HCL DOLGENCORP, LLC 69af44c2-390c-4223-889a-d5555aef5778 2026-08-28 Warnings Exact identifier application number: M012 acetaminophen extra strength ACETAMINOPHEN Sam's West Inc dd99efd0-4ca4-4dc6-a940-bebd17ac8f8d 2026-08-28 Warnings Exact identifier unii: 362O9ITL9D Tussin DM Daytime DEXTROMETHORPHAN HBR, GUAIFENESIN CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED 432d4833-2eaf-4f7c-b6b4-41043a6b7e2a 2026-08-28 Warnings Exact identifier application number: M012 unii: 9D2RTI9KYH unii: 495W7451VQ
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.